Blood sugar measuring device

ABSTRACT

The present invention is made to provide a safe and efficient blood glucose measuring device capable of collectively performing blood glucose measurement process and collectively performing insulin administration process on many patients, while ruling out the risk of misidentification and misprescription among the patients. When having read a patient ID with a patient ID reading section, a control section identifies a record of the patient of a measurement/administration results table. The control section does not perform blood glucose measurement on the patient of the identified record which shows that a blood glucose measurement flag is “true” and an insulin administration confirmation flag is “false”, and displays an insulin dosage on a display unit with respect to the patient by referring to a prescription information table based on the blood glucose level has been measured. The control section does not display the insulin dosage on the display unit again for the patient whose record is identified which shows that the insulin administration confirmation flag is “true”.

TECHNICAL FIELD

The present invention relates to a technique preferably applied to ablood sugar (glucose) measuring device.

More particularly, the present invention relates to a blood glucosemeasuring device capable of measuring blood glucose level for aplurality of patients and administering insulin to the patients inhospital in a rapid, safe and reliable manner.

BACKGROUND ART

As is well known, diabetes results from inappropriate secretion ofinsulin by the pancreas. Thus, it is necessary to measure the bloodglucose level for a diabetic patient before meals, and administerinsulin to the patient according to the measured level.

Conventionally, there has been a small sized blood glucose measuringdevice developed, manufactured and marketed by the applicant of thepresent invention, the blood glucose level being designed for measuringblood glucose of a patient at home by the patient himself/herself or bya family member of the patient. Patent applications relating to theblood glucose measuring device are disclosed in Patent Documents 1 and2.

[Patent Document 1] Japanese Unexamined Patent Application PublicationNo. H10-19888

[Patent Document 2] Japanese Unexamined Patent Application PublicationNo. H10-318928

DISCLOSURE OF THE INVENTION

Problems to be Solved by the Invention

It has been reported that the blood glucose measuring device designedfor home use is actually used as it is in clinical practice in hospitalswhere many patients are hospitalized.

However, the blood glucose measuring device designed for home use onlyhas a function of measuring blood glucose, and there are no safetymeasures for preventing accidents such as patient misidentification,duplicated administration of insulin and the like.

Further, in the blood glucose measuring device designed for home use,functions for improving efficiency of medical practice, such ascollectively performing blood glucose measurement process andcollectively performing insulin administration process on many patients,are not taken into consideration.

Nowadays, a new blood glucose measuring device having improved functionsin terms of safety, efficiency and the like is desired in order to meetthe needs of clinical practice.

The present invention is made in view of the above-mentioned problems,and an object of the present invention is to provide a safe bloodglucose measuring device capable of ruling out the risk ofmisidentification and misprescription among the patients.

Further, another object of the present invention is to provide a safeand efficient blood glucose measuring device capable of collectivelyperforming blood glucose measurement process and collectively performinginsulin administration process on many patients, while ruling out therisk of misidentification and misprescription among the patients.

To solve the aforesaid problems, a blood glucose measuring deviceaccording to an aspect of the present invention includes: a patient IDreading section for acquiring a patient ID assigned to a patient; ablood glucose measuring section for measuring blood glucose level of theblood drawn from the patient; a nonvolatile storage for storingpredetermined data; a prescription information table stored in thenonvolatile storage, the prescription information table havingprescription information stored therein in a manner in which theprescription information can be identified by the patient ID, theprescription information including kind and dosage of drugs for beingadministered corresponding to the blood glucose level of each of aplurality of patients; a search section for searching, with bloodglucose level and the patient ID, the prescription information table toacquire the prescription information of the patient; a display unit fordisplaying the prescription information acquired by the search section;an operating section for allowing an operator to input, in a state wherethe prescription information is displayed on the display unit, whetherthe prescription has been executed or not; and ameasurement/prescription results table stored in the nonvolatilestorage, the measurement/prescription results table having: a patient IDfield having the patient ID acquired by the patient ID reading sectionstored therein, a blood glucose level field for recording the bloodglucose level of the patient measured by the blood glucose measuringsection, a blood glucose measurement flag field for recording whetherthe blood glucose has been measured by the blood glucose measuringsection or not, and an insulin administration confirmation flag fieldfor recording whether the prescription has been executed or not afterthe prescription information has been displayed by the display unit.

To solve the aforesaid problems, the blood glucose measuring deviceaccording to the aforesaid aspect of the present invention furtherincludes: a recording section; and a control section, wherein, whenobtaining the blood glucose level from the blood glucose measuringsection, the recording section records the blood glucose level in theblood glucose level field and records a logical true in the bloodglucose measurement flag field of a record of themeasurement/prescription results table, the record being identified bythe patient ID, while when obtaining operation information from theoperating section, the recording section records a logical true in theinsulin administration confirmation flag field of the record, andwherein, after obtaining the patient ID by the patient ID readingsection, the control section confirms the blood glucose measurement flagfield and the insulin administration confirmation flag field of therecord, and if the blood glucose measurement flag field of the recordidentified by the patient ID of the measurement/prescription resultstable is “true” and the insulin administration confirmation flag fieldof the record is “false”, the control section will control the searchsection to obtain the prescription information, while if the bloodglucose measurement flag field of the record is “true” and the insulinadministration confirmation flag field of the record is “true”, thecontrol section will not control the search section to obtain theprescription information.

To solve the aforesaid problems, a blood glucose measuring deviceaccording to another aspect of the present invention includes: a patientID reading section for acquiring a patient ID assigned to a patient; ablood glucose measuring section for measuring the blood glucose level ofthe blood drawn from the patient; a nonvolatile storage for storingpredetermined data; a prescription information table stored in thenonvolatile storage, the prescription information table havingprescription information stored therein in a manner in which theprescription information can be identified by the patient ID, theprescription information including kind and dosage of drugs for beingadministered corresponding to the blood glucose level of each of aplurality of patients; a search section for searching, with bloodglucose level and the patient ID, the prescription information table toacquire the prescription information of the patient; a display unit fordisplaying the prescription information acquired by the search section;an operating section for allowing an operator to input, in a state wherethe prescription information is displayed on the display unit, whetherthe prescription has been executed or not; a measurement/prescriptionresults table stored in the nonvolatile storage, themeasurement/prescription results table having: a patient ID field havingthe patient ID stored therein, a blood glucose level field for recordingthe blood glucose level of the patient measured by the blood glucosemeasuring section, a blood glucose measurement flag field for recordingwhether the blood glucose has been measured by the blood glucosemeasuring section or not, and an insulin administration confirmationflag field for recording whether the prescription has been executed ornot after the prescription information has been displayed by the displayunit; a recording section; and a control section, wherein, whenobtaining the blood glucose level from the blood glucose measuringsection, the recording section records the blood glucose level in theblood glucose level field and records a logical true in the bloodglucose measurement flag field of a record of themeasurement/prescription results table, the record being identified bythe patient ID, while when obtaining operation information from theoperating section, the recording section records a logical true in theinsulin administration confirmation flag field of the record, andwherein, after reading the patient ID by the patient ID reading section,if the blood glucose measurement flag field of the record is “true” andthe insulin administration confirmation flag field of the record is“false”, the control section will cause the search section to search theprescription information table with the blood glucose level recorded inthe blood glucose level field of the record and the patient ID toacquire the prescription information and cause the display unit todisplay the prescription information.

The control section sets the measurement/prescription results table to“true” with respect to the patient who has received insulinadministration.

When performing blood glucose measurement again on the same patient, the“true” of the field of the insulin administration confirmation flag isdetected, and therefore insulin dosage will not be displayed.

Advantages of the Invention

According to the present invention, it is possible to provide a safeblood glucose measuring device capable of ruling out the risk ofmisidentification and misprescription among the patients.

Further, according to the present invention, it is possible to provide asafe and efficient blood glucose measuring device capable ofcollectively performing blood glucose measurement process andcollectively performing insulin administration process on many patients,while ruling out the risk of misidentification, such as duplicatedadministration of insulin, and misprescription among the patients.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a schematic view showing the overall configuration of a bloodglucose measuring system according to an embodiment of the presentinvention.

FIGS. 2A and 2B are perspective views showing the appearance of a bloodglucose meter according to the aforesaid embodiment of the presentinvention.

FIGS. 3A, 3B, 3C and 3D are views showing the blood glucose meteraccording to the aforesaid embodiment when viewed from four directions.

FIGS. 4A and 4B are views showing the appearance of a cradle in a statewhen the blood glucose meter is mounted thereon.

FIGS. 5A and 5B are views showing the appearance of the cradle in astate when the blood glucose meter is removed therefrom.

FIG. 6 is a block diagram showing the internal configuration of theblood glucose meter.

FIG. 7 is a block diagram showing the internal configuration of thecradle.

FIG. 8 is a block diagram showing connection state of the blood glucosemeter, the cradle and a measurement data management device.

FIG. 9 is a block diagram showing the measurement data managementdevice.

FIG. 10 is a schematic view showing the functions of the blood glucosemeter.

FIG. 11 is a functional block diagram showing a measurement conditioncheck section.

FIG. 12 is a functional block diagram showing a temperature judgingsection.

FIG. 13A is a functional block diagram showing a tip attachmentdetection section and FIG. 13B is a graph for explaining a mechanism fordetermining whether or not a measuring tip has been attached and whetheror not the measuring tip is a non-defective product.

FIG. 14 is a functional block diagram showing a blood glucose measuringsection.

FIG. 15 is a functional block diagram showing a prescription datadisplay section.

FIGS. 16A, 16B and 16C are schematic views showing tables stored in theblood glucose meter.

FIG. 17 is a state transition diagram showing screen transition of theblood glucose meter.

FIG. 18 is a partly enlarged view of the state transition diagram.

FIG. 19 is a partly enlarged view of the state transition diagram.

FIG. 20 is a partly enlarged view of the state transition diagram.

FIG. 21 is a partly enlarged view of the state transition diagram.

FIGS. 22A, 22B and 22C are schematic views showing nurse's workflow andattendant screen transition of the blood glucose meter.

FIGS. 23D, 23E and 23F are schematic views showing nurse's workflow andattendant screen transition of the blood glucose meter.

FIGS. 24G, 24H, 24I and 24J are schematic views showing nurse's workflowand attendant screen transition of the blood glucose meter.

FIGS. 25K, 25L, 25M and 25N are schematic views showing nurse's workflowand attendant screen transition of the blood glucose meter.

FIGS. 26O, 26P and 26Q are schematic views showing nurse's workflow andattendant screen transition of the blood glucose meter.

FIGS. 27R and 27S are schematic views showing nurse's workflow andattendant screen transition of the blood glucose meter.

FIG. 28 is a flowchart showing the flow of the overall operation of theblood glucose meter.

FIG. 29 is a flowchart showing the flow of a measurement process of theblood glucose meter.

FIG. 30 is a flowchart showing the flow of the measurement process ofthe blood glucose meter.

FIG. 31 is a flowchart showing the flow of a patient ID scanningprocess.

FIG. 32 is a flowchart showing the flow of the patient ID scanningprocess.

FIG. 33 is a flowchart showing the flow of a user ID scanning process.

FIG. 34 is a flowchart showing the flow of the user ID scanning process.

FIG. 35 is a flowchart showing the flow of a tip lot scanning process.

FIG. 36 is a flowchart showing the flow of the tip lot scanning process.

FIG. 37 is a flowchart showing the flow of a tip attaching process.

FIG. 38 is a flowchart showing the flow of a measurement executionprocess.

FIG. 39 is a flowchart showing the flow of a prescription displayprocess.

FIG. 40 is a flowchart showing the flow of the prescription displayprocess.

FIG. 41 is a partly enlarged view of screen transition diagram based onan application example.

FIG. 42 is a partly enlarged view of the flowchart based on theapplication example.

FIG. 43 is a partly enlarged view of screen transition diagram based onthe application example.

FIG. 44 is a partly enlarged view of the flowchart based on theapplication example.

BEST MODES FOR CARRYING OUT THE INVENTION

An embodiment of the present invention will be described below withreference to FIGS. 1 to 44.

[Blood Glucose Measuring System 101]

FIG. 1 is a schematic view showing the overall configuration of a bloodglucose measuring system according to an embodiment of the presentinvention.

A blood glucose measuring system 101 includes a blood glucose meter 102,which is a blood glucose measuring device, a cradle 103 and ameasurement data management device 104.

The blood glucose meter 102 is a portable device that basically fits inthe palm of an adult hand and that is operated using a secondary batterysuch as a lithium-ion secondary battery.

In the case where the blood glucose level of a patient is measured by adoctor, a nurse or the like, generally the blood glucose meter 102 isbrought into a ward of a hospital, and a tiny amount of blood is drawnfrom the patient to measure the blood glucose level. The blood drawingprocess and the blood glucose measurement process are performedfollowing the steps of: sticking the tip of a finger of the patient witha puncture tool, and causing the blood exuded from the fingertip to besoaked into a measuring tip attached to the blood glucose meter 102.

Make sure that the blood glucose meter 102 is mounted on the cradle 103after performing the blood glucose measurement and insulinadministration.

In addition to charging the battery of the blood glucose meter 102, thecradle 103 also functions as an interface through which the bloodglucose meter 102 transmits/receives data to/from the measurement datamanagement device 104.

The partner to/from which the blood glucose meter 102 transmits/receivesdata through the cradle 103 is the measurement data management device104.

The measurement data management device 104, which is configured by apersonal computer, is connected with the cradle 103 through a USB cable105.

A known OS operates to execute the measurement data management device104. Further, a program for causing the computer to function as themeasurement data management device 104 operates under the OS.

As soon as the blood glucose meter 102 is mounted on the cradle 103, thecommunication between the blood glucose meter 102 and the measurementdata management device 104 is performed through the cradle 103, and abelow-mentioned measurement/prescription results table is transmitted tothe measurement data management device 104.

Further, below-mentioned various tables can be uploaded to the bloodglucose meter 102 from the measurement data management device 104.

The details about these tables will be described later.

[Appearance: Blood Glucose Meter 102]

FIGS. 2A and 2B are perspective views showing the appearance of theblood glucose meter 102.

FIGS. 3A, 3B and 3C are views showing the blood glucose meter whenviewed from four directions.

In order to facilitate description, the surface where an LCD is provided(as shown in FIGS. 2A and 3A) is referred to as a “body front surface”hereinafter, and the surface where a battery lid is provided (as shownin FIG. 2B) is referred to as a “body rear surface”.

As shown in FIGS. 3A and 3C, an optical measuring section 202 isprovided at the tip end of the blood glucose meter 102.

The optical measuring section 202 has a shape allowing a blood glucosemeasuring tip 212 (referred to as “measuring tip 212” hereinafter) to beattached and detached. The used measuring tip 212 can be detached fromthe optical measuring section 202 by operating an eject lever 302.

As shown in FIG. 2A and FIG. 3A, a power switch 204, Cursor keys 205, anEnter key 206 and a Bar-code key 207 are arranged on the side surface(the body front surface) where the LCD 203 (a liquid crystal display) isprovided, at positions beside the LCD 203.

The power switch 204 is used to switch on and off the power of the bloodglucose meter 102.

The Cursor keys 205 are used to move the cursor to select one of aplurality of items displayed on the LCD 203.

The Enter key 206 is used to issue an instruction for “executing” or“selecting” the item selected by the cursor.

The Bar-code key 207 is used to cause a bar-code reader 208 shown inFIG. 3D to operate, wherein the bar-code reader 208 is arranged on aside of the blood glucose meter 102 opposite to the side where theoptical measuring section 202 is arranged.

The bar-code reader 208 is a bar-code reading device configured by acombination of a known red laser diode and a light-receiving elementsuch as a phototransistor. Incidentally, an image sensor such as a CCD,a CMOS or the like can be used instead of the light-receiving element.

The basic mechanism of the blood glucose meter 102 for measuring bloodglucose is identical to that of the conventional arts, and will bebriefly described below.

The measuring tip 212 is attached to the optical measuring section 202,the fingertip of the patient is stuck with a puncture tool, and theblood exuded from the fingertip is soaked into the measuring tip 212. Atest paper made of a porous membrane such as a polyether sulfonemembrane is provided inside the measuring tip 212. Further, when theblood soaked into the measuring tip 212 is permeated into the testpaper, the blood will be reacted with the reagent contained in the testpaper, so that the test paper develops a color. The color reactionrequires about several to ten and several seconds, and the reaction timeis affected by the ambient temperature.

After a predetermined reaction time has elapsed, a light-emittingelement is caused to emit light, the light emitted from thelight-emitting element irradiate to the test paper, and the lightreflected from the test paper is received by the light-receivingelement. Further, an analog light-receiving intensity signal obtainedfrom the light-receiving element is converted into a digital value, andthereafter the digital value is converted into the blood glucose levelto be displayed on the LCD 203.

Incidentally, the mechanism of blood glucose measurement on the side ofthe blood glucose meter 102 is not limited to the aforesaid opticalmeasurement method in which a coloring reagent is used, but may be anyother methods possible to be used to perform the conventional bloodglucose measurement, such as an electrochemical sensor method or thelike.

As shown in FIG. 2B, a power terminal 209 and an infrared communicationwindow 210 are provided in the body rear surface on the side of thebar-code reader 208. When the blood glucose meter 102 is mounted on thecradle 103, the power terminal 209 is brought into contact with acharging terminal 402 (see FIGS. 4A and 4B) provided in the cradle 103,so that the blood glucose meter 102 is charged while an infraredcommunication between the blood glucose meter 102 and the cradle 103 isperformed. Incidentally, the battery lid 211 is also provided on thebody rear surface.

[Appearance: Cradle 103]

FIGS. 4A and 4B are views showing the appearance of the cradle 103 in astate when the blood glucose meter 102 is removed therefrom, and FIGS.5A and 5B are views showing the appearance of the cradle 103 in a statewhen the blood glucose meter 102 is mounted thereon.

As shown in FIGS. 4A and 4B, the charging terminal 402 is arranged inthe cradle 103 at a position corresponding to the power terminal 209 ofthe blood glucose meter 102. Similarly, an infrared communication window403 is arranged in the cradle 103 at a position corresponding to theinfrared communication window 210 of the blood glucose meter 102.

An infrared light-emitting diode and a phototransistor are providedinside both the infrared communication window 210 of the blood glucosemeter 102 and the infrared communication window 403 of the cradle 103.These components constitute a known IrDA (Infrared Data Association)based infrared serial communication interface.

As shown in FIG. 1, the cradle 103 is connected to the measurement datamanagement device 104 through the USB cable 105. The cradle 103 has afunction of charging the battery of the blood glucose meter 102. Sinceit is possible to connect many cradles 103 to the measurement datamanagement device 104, the cradle 103 is configured as a self-powereddevice which does not receive power supply from a USB terminal of themeasurement data management device 104.

[Hardware: Blood Glucose Meter 102]

FIG. 6 is a block diagram showing the internal configuration of theblood glucose meter 102.

The blood glucose meter 102 includes a CPU 602, a ROM 603, a RAM 604,and a bus 605 for connecting the CPU 602, the ROM 603 and the RAM 604.In addition to the aforesaid components, a section for providing a datainput function and a section for providing a data output function arealso connected to the bus 605.

For sake of convenience, hereinafter the CPU 602, the ROM 603, the RAM604 and the bus 605 are referred to as a microcomputer that constitutesthe blood glucose meter 102.

The section for providing a data input function of the blood glucosemeter 102 includes the optical measuring section 202 for obtaining bloodglucose measurement data, a thermistor 606 for obtaining temperaturedata, the bar-code reader 208, a calendar clock 607, and an operatingsection 608.

The optical measuring section 202 includes a light-emitting portion anda light-receiving portion, wherein the light-emitting portion includes alight-emitting diode 609, a driver 610 of the light-emitting diode 609,and a D/A converter 611 connected to the driver 610, and thelight-receiving portion includes a phototransistor 612 and an A/Dconverter 613.

Since the test paper arranged inside the measuring tip 212 needs to beirradiated by light of a suitable intensity, the light-emitting diode609 is controlled so as to emit light based on light-emitting intensitydata stored in a below-mentioned nonvolatile storage 614. In otherwords, the light-emitting intensity data is read out from thenonvolatile storage 614, converted into an analog voltage signal by theD/A converter 611, and then power-amplified by the driver 610 to drivethe light-emitting diode 609 to emit light.

On the other hand, a signal voltage of intensity of the light receivedby the phototransistor 612 is converted into digital data by the A/Dconverter 613. Further, the converted digital data is converted intoblood glucose level data by performing a predetermined arithmeticprocess executed by the CPU 602, and then the blood glucose level datais recorded in a predetermined area of the RAM 604 and a predeterminedarea of the nonvolatile storage 614.

Further, the blood glucose meter 102 has the thermistor 606, and ambienttemperature of the blood glucose meter 102 can be measured based on thechange of the resistance of the thermistor 606. Similar to thephototransistor 612, the resistance of the thermistor 606 is convertedinto digital data by the A/D converter 613, and the digital data isstored in a predetermined area of the RAM 604 and a predetermined areaof the nonvolatile storage 614. Incidentally, since it is not necessaryto simultaneously measure the light-receiving intensity and thetemperature, the A/D converter 613 can be shared by the phototransistor612 and the thermistor 606.

The bar-code reader 208 causes a red laser diode 622 to emit light, thereflected light is received by a phototransistor 623 so that thebar-code is read, and the data recorded on the bar-code is outputted tothe bus 605.

The calendar clock 607 is a known IC also called as a “real-time clock”which provides a date and time data output function, and is mounted asstandard on many microcomputers, personal computers and the like.

In the blood glucose meter 102 according to the present embodiment ofthe present invention, since it is necessary to acquire informationregarding the date and time when the blood glucose was being measured,date and time information is important information. In other words, thedata to be collected and the date and time information have very closerelation with each other. Further, the date and time information whenthe blood glucose was being measured needs to be stored in ameasurement/prescription results table 1408 (which is to be describedlater with reference to FIG. 14) along with the blood glucose level. Forthis reason, the calendar clock 607 is daringly shown in the drawings.

The operating section 608 is a known key switch formed by push-buttons,the operating section 608 including the Cursor keys 205 and the Enterkey 206. The operating section 608 is used for a user to operate theblood glucose meter 102 according to the content displayed on abelow-mentioned display unit 615 which is a LCD.

The section for providing a data output function of the blood glucosemeter 102 includes the display unit 615 configured by the LCD 203, abuzzer 616 and an infrared communication section 617.

Various screens are displayed on the display unit 615 by a programstored in the ROM 603 and executed by the CPU 602. The details aboutdisplay screens will be described later.

The buzzer 616 is mainly used to notify the user that the bar-codereader 208 has successfully read the bar-code, that the measurementoperation of the blood glucose measurement has completed, that theinfrared communication has completed, or that an error message isdisplayed. The buzzer 616 may also sound every time when operating theoperating section 608 depending on setting.

As mentioned above, an infrared light-emitting diode 619 and aphototransistor 620 are connected to the infrared communication section617, and these components constitute an IrDA based serial interface.When detecting that the blood glucose meter 102 has received powersupply from the cradle 103 based on voltage changing of the powerterminal 209, the power circuit 618 reports this fact to the CPU 602through the bus 605. Further, based on the control of the CPU 602, theinfrared communication function of the infrared communication section617 is started, so that if the infrared communication between the bloodglucose meter 102 and the cradle 103 is performed, the various tablesstored in the nonvolatile storage 614 will transmits/receives datato/from the measurement data management device 104 and thereby thesetables are updated.

In other words, when performing the infrared communication between theblood glucose meter 102 and the cradle 103, the infrared communicationis immediately executed as soon as the blood glucose meter 102 ismounted on the cradle 103 without needing to operate the operatingsection 608 and the like of the blood glucose meter 102.

In addition to the data output function, the blood glucose meter 102 isprovided with the nonvolatile storage 614 (which is an EEPROM) thatprovides data storage function. A patient table 1109, a user table 1113,a tip lot table 1117, a prescription information table 1502, ameasurement/prescription table 1602, a measurement/prescription resultstable 1408 and the like (all these tables are to be described later withreference to FIGS. 11, 14, 15, 16A, 16B and 16C) are stored in thenonvolatile storage 614. These tables are updated when the communicationbetween the blood glucose meter 102 and the measurement data managementdevice 104 is performed through the cradle 103. Incidentally, a flashmemory may also be used instead of the EEPROM.

[Hardware: Cradle 103]

FIG. 7 is a block diagram showing the internal configuration of thecradle 103.

FIG. 8 is a view schematically showing connection state of the bloodglucose meter 102, the cradle 103 and the measurement data managementdevice 104.

As shown in FIG. 7, the cradle 103 includes a CPU 702, a ROM 703, a RAM704, an infrared communication section 717, a USB interface (I/F) 706, acharging circuit 718 and a bus 705 which connects these components,wherein the CPU 702, the ROM 703 and the RAM 704 constitute amicrocomputer, and the infrared communication section 717 has aninfrared light-emitting diode 719 and a phototransistor 720 connectedthereto.

When detecting that the blood glucose meter 102, which is a load, isconnected based on voltage changing of the charging terminal 402, thecharging circuit 718 reports this fact to the CPU 702 through the bus705. Further, based on the control of the CPU 702, the infraredcommunication function of the infrared communication section 717 isstarted, so that the communication between the blood glucose meter 102and the measurement data management device 104 is performed through theinfrared communication section 717 and the USB interface 706.

As described above, the blood glucose meter 102 and the cradle 103 areconnected with each other through the IrDA, and the cradle 103 and themeasurement data management device 104 are connected with each otherthrough the USB. From this aspect, the cradle 103 serves as an interfaceto enable data communication between the measurement data managementdevice 104 and the blood glucose meter 102.

[Hardware: Measurement Data Management Device 104]

FIG. 9 is a block diagram showing the measurement data management device104.

As described above, the measurement data management device 104 isactually a known personal computer.

A bus 902 is provided inside the measurement data management device 104.A CPU 903, a ROM 904, a RAM 905, a nonvolatile storage (such as a harddisk device or the like) 906, a display unit (such as a LCD or the like)907 and a USB interface (I/F) 908 are connected to the bus 902. Inaddition to an operating section (such as a keyboard, a mouse and/or thelike) 909, the cradle 103 is connected to the USB interface 908.

[Software: Blood Glucose Meter 102]

FIG. 10 is a schematic view showing the functions of the blood glucosemeter 102. FIG. 10 shows the functions executed by a program stored inthe ROM 603 of the microcomputer. Note that FIG. 10 is not a functionalblock diagram for explaining the details of the functions.

When the microcomputer executes the program, the blood glucose meter 102is brought into a state capable of performing four functions.

First, the microcomputer causes the blood glucose meter 102 to functionas a measurement condition check section 1002 for checking themeasurement condition of the blood glucose, together with peripheraldevices such as the bar-code reader 208 and the like.

Next, the microcomputer causes the blood glucose meter 102 to functionas a blood glucose measuring section 1003 for actually measuring theblood glucose, together with peripheral devices such as the opticalmeasuring section 202 and the like.

Finally, the microcomputer causes the blood glucose meter 102 tofunction as a prescription data display section 1004 for displayingprescription data obtained based on the measured blood glucose level.

In the case where the blood glucose measurement is performed for each ofpatients one by one and the insulin prescription is performed for eachof patients one by one, the aforesaid function states are repeated.

In addition to the aforesaid operation procedure, the blood glucosemeter 102 according to the present embodiment may also operate inaccordance with an operation procedure in which the blood glucosemeasurement is collectively performed for each of patients, andthereafter the insulin prescription is collectively performed for eachof patients. Such procedure is shown as a flow indicated by arrows R1005and R1006 of the dotted line of FIG. 10.

In any one of the aforesaid three function states, the microcomputercauses the blood glucose meter 102 to function as a data communicatingsection 1007 as soon as the blood glucose meter 102 is mounted on thecradle 103, so that it is possible to transfer data files between theblood glucose meter 102 and the measurement data management device 104.

Incidentally, FIG. 10 may also be viewed as a state transition diagramshowing operation state of the blood glucose meter 102, as well as afunctional block diagram. To be specific:

When functioning as the measurement condition check section 1002, theblood glucose meter 102 displays a message “measurement condition checkstate”;

When functioning as the blood glucose measuring section 1003, the bloodglucose meter 102 displays a message “blood glucose measurement state”;

When functioning as the prescription data display section 1004, theblood glucose meter 102 displays a message “prescription data displaystate”; and

When functioning as the data communicating section 1007, the bloodglucose meter 102 displays a message “data communication state”.

FIGS. 11, 12, 13A, 13B, 14 and 15 are block diagrams showing thefunctions achieved by executing the program stored in the ROM 603 of themicrocomputer.

FIG. 11 is a functional block diagram showing the measurement conditioncheck section 1002.

The measurement condition check section 1002 sequentially checks sixmeasurement conditions.

A QC check section 1103 checks whether or not a QC check of the bloodglucose meter 102 is normally completed within a predetermined period.

The QC check is a process to be periodically executed mainly in order tomaintain blood glucose measurement accuracy. To be more specific, theconcrete purpose of the QC check is adjusting the light-emittingintensity of the light-emitting diode 609 and amplification gain of thephototransistor 612 of the optical measuring section 202. The concreteoperation steps of the QC check includes: attaching an adjustment tipinstead of the measuring tip 212, causing the adjustment tip to soak anadjustment reagent, and performing adjustment so that the light-emittingdiode 609 obtains a suitable light-emitting intensity.

A predetermined date interval value 1104 is a text file stored in thenonvolatile storage 614, and a date interval of QC check is recorded inthe predetermined date interval value 1104, wherein the date interval ofQC check is set by the nurse or the like when he or she performs aset-up procedure of the system.

A QC check record 1105 is a text file stored in the nonvolatile storage614, and the date and time when the last QC check was performed isrecorded in the QC check record 1105.

A judging section 1106 compares the record of the QC check record 1105with a current date and time obtained from the calendar clock 607 tojudge whether or not the QC check has been performed within the dateinterval of QC check recorded in the predetermined date interval value1104. For example, in the case where “one week” is set for thepredetermined date interval value 1104, if the QC check is not performedfor seven days or longer, the judging section 1106 will give a warn.

A patient ID reading section 1107 reads a patient ID with the bar-codereader 208, and searches the patient table 1109 with a search section1110 to see whether or not the patient ID exists in the patient table1109.

The read patient ID is stored in a patient ID variable 1108.

A user ID reading section 1111 reads a user ID with the bar-code reader208, and searches the user table 1113 with a search section 1114 to seewhether or not the user ID exists in the user table 1113.

The read user ID is stored in a user ID variable 1112.

A tip lot reading section 1115 reads a tip lot (a lot number of themeasuring tip) of the measuring tip 212 attached to the opticalmeasuring section 202 with the bar-code reader 208, and judges, with ajudging section 1118, whether or not the tip lot exists in tip lot table1117 and whether or not the measuring tip 212 is within the validitydate.

The read tip lot is stored in a tip lot variable 1116.

Incidentally, the patient ID reading section 1107, the user ID readingsection 1111 and the tip lot reading section 1115 share the bar-codereader 208 through a switch 1116.

A temperature check section 1119 measures the temperature with thethermistor 606, converts the measured result into digital data, and thenjudges whether or not the temperature data is within an allowable rangewith a temperature judging section 1120.

The temperature data obtained by performing the measurement is stored ina temperature variable 1122.

After the measuring tip 212 is attached, a tip attachment check section1123 judges whether or not the attached measuring tip 212 is deemed anew one.

The light-emitting intensity stored in an adjustment value (which is atext file) 1125 stored in the nonvolatile storage 614 is converted intoan analog voltage signal by the D/A converter 611 and thenpower-amplified by the driver 610 to drive the light-emitting diode 609to emit light. Further, the light of the light-emitting diode 609 isirradiated to a test piece 1127 inside the measuring tip 212, the lightreflected from the measuring tip 212 is signal-converted by thephototransistor 612, the result is converted into digital data by theA/D converter 613, and then a tip attachment detection section 1124judges whether or not a new measuring tip 212 has been normallyattached.

A control section 1128 sequentially causes the QC check section 1103,the patient ID reading section 1107, the user ID reading section 1111,the tip lot reading section 1115, the temperature check section 1119 andthe tip attachment check section 1123 to operate, and obtains executionresults of these sections. Therefore, the control section 1128 controlsthe switch 1116, a switch 1121 and a switch 1126.

Further, the control section 1128 receives the operations of the userwith the operating section 608, and displays various execution resultson the display unit 615.

FIG. 12 is a functional block diagram showing the temperature judgingsection 1120.

The temperature data obtained from the thermistor 606 through the A/Dconverter 613 is inputted to two comparators 1202 and 1203, and whetheror not the temperature data falls in a range between an upper limit 1204and a lower limit 1205 is judged as an output of an AND gate 1206.

FIG. 13A is a functional block diagram showing the tip attachmentdetection section 1124, and FIG. 13B is a graph for explaining amechanism for determining whether or not the measuring tip 212 has beenattached and whether or not the measuring tip 212 is a non-defectiveproduct.

The reflected light data obtained from the measuring tip 212 through theA/D converter 613 is held by two sample-and-hold circuits 1302 and 1303.The holding timings are controlled by a clock 1304. In other words, thesample-and-hold circuit 1302 and the sample-and-hold circuit 1303respectively hold values obtained at timings shifted by one sampleclock.

The value of the sample-and-hold circuit 1302 and the value of thesample-and-hold circuit 1303 are compared with each other by acomparator 1305.

The sample-and-hold circuit 1302, the sample-and-hold circuits 1303, theclock 1304 and the comparator 1305 constitute a rising edge detectionsection 1309 for detecting a rising edge of the reflected light data.

When the value of the reflected light data rises, the comparator 1305indicates positive. In response to this, a switch 1306 is controlled toturn on.

The value of the sample-and-hold circuit 1302 at this time is comparedwith a threshold 1308 by a comparator 1307 to judge whether or not thereflection light intensity is sufficient.

Operation for judging whether or not the measuring tip 212 has beenattached and whether or not the measuring tip 212 is a non-defectiveproduct will be described below with reference to FIG. 13B.

Supposing that a nurse has attached a used measuring tip 212 by mistake,since the test piece inside the measuring tip 212 had been reacted andtherefore has a reduced reflectance, the reflection light intensity willbe lower than the threshold.

First, the reflection light intensity value is obtained respectively attime t1 and time t2, and the rising edge of the reflection lightintensity is detected by comparing the obtained values. This is thefunction of the rising edge detection section 1309.

Next, the reflection light intensity value obtained at time t2 iscompared with the threshold to confirm that a new measuring tip 212 hasbeen attached. This is the function of the comparator 1307.

FIG. 14 is a functional block diagram showing the blood glucosemeasuring section 1003.

An adjustment value data 1402 stored in the nonvolatile storage 614 issupplied, through a switch 1403, to the D/A converter 611 where the datais converted into an analog voltage signal. The analog voltage signaldrives the driver 610, which is a power amplifier, to control thelight-emitting intensity of the light-emitting diode 609.

The light emitted by the light-emitting diode 609 is irradiated to thetest piece 1127 provided inside the measuring tip 212. Thephototransistor 612 of the optical measuring section 202 receives thelight reflected from the test piece 1127, and converts the reflectedlight into a voltage signal.

The voltage signal obtained from the phototransistor 612 is convertedinto a digital value by the A/D converter 613. A detection section 1404verifies the digital value and performs a predetermined arithmeticprocess to convert the digital value into a blood glucose level.

The blood glucose level is stored in a blood glucose level variable 1405provided in the RAM 604.

A judging section 1406 verifies whether the value of the blood glucoselevel variable 1405 is extremely large or extremely small. Further, thevalue of the blood glucose level variable 1405 is supplied to thecontrol section 1128 to be used to display the blood glucose level onthe display unit 615. At this time, the judgment result of the judgingsection 1406 is reflected by the display content of the display unit615.

A recording section 1407 records the following data in themeasurement/prescription results table 1408 stored in the nonvolatilestorage 614 in a predetermined format: the current date and time dataobtained from the calendar clock 607, the patient ID variable 1108, theuser ID variable 1112, the tip lot variable 1116, the temperaturevariable 1122 and the blood glucose level variable 1405, wherein thepatient ID variable 1108, the user ID variable 1112, the tip lotvariable 1116, the temperature variable 1122 had been previouslyobtained by the measurement condition check section 1002.

FIG. 15 is a functional block diagram showing the prescription datadisplay section 804.

The control section 1128 controls a search section 1505 to read out therecorded blood glucose level data from the measurement/prescriptionresults table 1408.

Using the patient ID variable 1108 as a search key, the search section1505 reads out the blood glucose level data of the patient recorded inthe measurement/prescription results table 1408 by the blood glucosemeasuring section 1003, and writes the blood glucose level data to ablood glucose measurement value 1506, which is a temporary variable.

The control section 1128 controls a search section 1503 to read out theprescription data from the prescription information table 1502 stored inthe nonvolatile storage 614.

Using the patient ID variable 1108 and the blood glucose measurementvalue 1506 as search keys, the search section 1503 reads out theprescription data of the patient (namely, insulin dosage and drug name)stored in the prescription information table 1502, and transfers theprescription data to the control section 1128.

The drug name and the insulin dosage obtained through the search section1503 are displayed on the display unit 615 through the control section1128.

After displaying the prescription data on the display unit 615, thecontrol section 1128 controls the recording section 1407 to record theprescription data (the insulin dosage and drug name) in a record of thepatient in the measurement/prescription results table 1408, and rewritesan insulin administration confirmation flag.

The details about the recording section 1407 will be described laterwith reference to FIGS. 16A to 16C.

[Various Tables: Blood Glucose Meter 102]

The main tables stored in the blood glucose meter 102 or to be made willbe described below.

FIGS. 16A to 16C are schematic views showing tables stored in the bloodglucose meter 102.

FIG. 16A is a list of the fields of the measurement/prescription table1602.

The measurement/prescription table 1602 is transmitted from themeasurement data management device 104 to the blood glucose meter 102,and an instruction on blood glucose measurement procedure and/or aninstruction on insulin administration procedure are recorded on themeasurement/prescription table 1602.

A number for uniquely identifying the patient is stored in a “PATIENTID” field.

A scheduled measurement time created by the measurement data managementdevice 104 is stored in a “SCHEDULED MEASUREMENT TIME” field. Thescheduled measurement time is used as a search key for identifyingwhether or not the blood glucose measurement should be performed andidentifying the number of prescriptions in the measurement datamanagement device 104 when transmitting data to the measurement datamanagement device 104.

A flag indicating an instruction on whether the blood glucose should bemeasured is stored in a “BLOOD GLUCOSE MEASUREMENT FLAG” field.

A value indicating an instruction on whether insulin (drug) should beadministered, and if yes, how many kinds of administration should beperformed is stored in a “PRESCRIPTION NUMBER” field.

After the blood glucose of the patient is measured, the number of thekind of the insulin to be administered to the patient is not limited toone. Thus, the blood glucose meter 102 is configured so that up to threekinds of prescriptions can be applied to the patient.

The “PRESCRIPTION NUMBER” field can take different values correspondingto the number of the prescribe drugs from “0”, which means the patientonly receives blood glucose measurement without receiving anyprescription, to “3”, which means three kinds of drugs are prescribed tothe patient.

FIG. 16B is a list of the fields of the measurement/prescription resultstable 1408.

The measurement/prescription results table 1408 is a table in which theresults of the blood glucose measurement and the contents (executionresults) of the insulin administration performed by the blood glucosemeter 102 are recorded. The measurement/prescription results table 1408is in pair relation with the measurement/prescription table 1602 inwhich the contents (instruction) executed by the blood glucose meter 102are described.

The date and time when the blood glucose was measured is recorded in a“DATE AND TIME OF MEASUREMENT” field. The date and time is recorded byacquiring the date and time by the calendar clock 607 in the recordingsection 1407 of the blood glucose measuring section 1003.

Similar to the “PATIENT ID” field of the measurement/prescription table1602, a number for uniquely identifying the patient is stored in a“PATIENT ID” field of the measurement/prescription results table 1408.

A number for uniquely identifying the user is stored in a “USER ID”field.

A tip lot number is recorded in a “TIP LOT” field.

The temperature when the blood glucose was measured is recorded in a“TEMPERATURE” field.

The patient ID variable 1108, the user ID variable 1112, the tip lotvariable 1116 and the temperature variable 1122, each being obtained bythe measurement condition check section 1002, are respectively recordedin a “PATIENT ID” field, a “USER ID” field, a “TIP LOT” field and a“TEMPERATURE” field.

A measured blood glucose level is recorded in a “BLOOD GLUCOSE LEVEL”field. To be specific, the content of the blood glucose level variable1405 obtained by the blood glucose measuring section 1003 is recorded.

A flag indicating whether or not the blood glucose has been measured isrecorded in a “BLOOD GLUCOSE MEASUREMENT. FLAG” field.

Similar to the “SCHEDULED MEASUREMENT TIME” field of themeasurement/prescription table 1602, a scheduled measurement timecreated by the measurement data management device 104 is stored in a“SCHEDULED MEASUREMENT TIME” field of the measurement/prescriptionresults table 1408. In other words, the content of the “SCHEDULEDMEASUREMENT TIME” field of the measurement/prescription results table1408 is copied from the “SCHEDULED MEASUREMENT TIME” field of themeasurement/prescription table 1602.

Similar to the “PRESCRIPTION NUMBER” field of themeasurement/prescription table 1602, a value indicating an instructionon whether the insulin should be administered, and if yes, how manykinds of administration should be performed is stored in a “NUMBER OFINSULIN ADMINISTRATIONS” field. In other words, the content of the“NUMBER OF INSULIN ADMINISTRATIONS” field of themeasurement/prescription results table 1408 is copied from the“PRESCRIPTION NUMBER” field of the measurement/prescription table 1602.

An “INSULIN ADMINISTRATION INFORMATION” field consists of four fields,which are a “DRUG NAME” field, an “INSULIN DOSAGE” field, an “INSULINDOSAGE DISPLAY FLAG” field and an “INSULIN ADMINISTRATION CONFIRMATIONFLAG” field, and is a variable-length field having a plurality ofrecords, wherein the number of the records is equal to the numberindicated in the “NUMBER OF INSULIN ADMINISTRATIONS” field.

A drug name of insulin is recorded in a “DRUG NAME” field.

An insulin dosage obtained by referring to the prescription informationtable 1502 based on the measured blood glucose level is stored in the“INSULIN DOSAGE” field. To be specific, the content of the prescriptiondata, which is acquired by the search section 1503 in the prescriptiondata display section 804 and recorded by the control section 1128 whendisplaying the prescription data on the display unit 615, is recorded inthe “INSULIN DOSAGE” field.

A flag indicating whether or not the insulin dosage has been displayedon the display unit is recorded in the “INSULIN DOSAGE DISPLAY FLAG”field.

A flag indicating whether or not the insulin has been administered isrecorded in the “INSULIN ADMINISTRATION CONFIRMATION FLAG” field.

As mentioned above when describing the “PRESCRIPTION NUMBER” field ofthe measurement/prescription table 1602, the “NUMBER OF INSULINADMINISTRATIONS” field can also take different values from “0” to “3”.

If the “NUMBER OF INSULIN ADMINISTRATIONS” field is “0”, the “INSULINADMINISTRATION INFORMATION” field itself does not exist.

If the “NUMBER OF INSULIN ADMINISTRATIONS” field is “1”, there will beone record in the “INSULIN ADMINISTRATION INFORMATION” field, the recordconsisting of four fields which are a “DRUG NAME” field, an “INSULINDOSAGE” field, an “INSULIN DOSAGE DISPLAY FLAG” field and an “INSULINADMINISTRATION CONFIRMATION FLAG” field.

Similarly, if the “NUMBER OF INSULIN ADMINISTRATIONS” field is “2”,there will be two records in the “INSULIN ADMINISTRATION INFORMATION”field, and if the “NUMBER OF INSULIN ADMINISTRATIONS” field is “3”,there will be three records in the “INSULIN ADMINISTRATION INFORMATION”field.

The prescription result for one patient is recorded in one record of themeasurement/prescription results table 1408. Thus, there are up to threeinsulin dosage display flags and up to three insulin administrationconfirmation flags existed in one record respectively for each kind ofdrugs to be administered to the patient.

Upon receiving the measurement/prescription table 1602 from themeasurement data management device 104, the blood glucose meter 102 oncestores the measurement/prescription table 1602 in the nonvolatilestorage 614.

Next, based on the contents described in the measurement/prescriptiontable 1602, the blood glucose meter 102 creates themeasurement/prescription results table 1408 in the nonvolatile storage614.

First, the “PATIENT ID” field and the “SCHEDULED MEASUREMENT TIME” fieldof the measurement/prescription results table 1408 are copied from the“PATIENT ID” field and the “SCHEDULED MEASUREMENT TIME” field of themeasurement/prescription table 1602.

Next, if the blood glucose measurement flag of themeasurement/prescription table 1602 is “true”, the blood glucosemeasurement flag of the measurement/prescription results table 1408 willbe set to “false”.

Inversely, if the blood glucose measurement flag of themeasurement/prescription table 1602 is “false”, the blood glucosemeasurement flag of the measurement/prescription results table 1408 willbe set to “true”.

Next, the number of prescriptions of the measurement/prescription table1602 is copied to the number of insulin administrations of themeasurement/prescription results table 1408.

Further, in response to the number of prescriptions of themeasurement/prescription table 1602, a plurality of records are createdin the “INSULIN ADMINISTRATION INFORMATION” field of themeasurement/prescription results table 1408, the number of the recordsis equal to the number of prescriptions of the measurement/prescriptiontable 1602. At this time, initial value of both the insulin dosagedisplay flag and the insulin administration confirmation flag is set to“false”.

By performing the aforesaid process for all records of themeasurement/prescription table 1602, a plurality of records are createdin the measurement/prescription results table 1408, wherein the numberof the records is equal to the number of those of themeasurement/prescription table 1602.

FIG. 16C shows an example of the records recorded in the prescriptioninformation table 1502.

The prescription information table 1502 is a table in which instructioninformation on dosage of insulin according to some known sliding scaleis recorded. The prescription information table 1502 is a table in whichthe blood glucose level range and the insulin dosage corresponding tothe blood glucose level range correspond each other.

There are a plurality of records of one patient ID in the “PATIENT ID”field. At least any one of a “CLASSIFICATION NUMBER” field, a “BLOODGLUCOSE LEVEL RANGE” field, a “DRUG NAME” field and a “PRESCRIPTION”field of these records have different values.

The “CLASSIFICATION NUMBER” field corresponds to the kind of the drugs,and has the minimum value of “1” and the maximum value of “3”. The valueof the “CLASSIFICATION NUMBER” field and the “DRUG NAME” fieldcorrespond one-to-one with each other.

In an example shown in FIG. 16C, a patient having patient ID “123456”has nine records whose classification numbers are “1”. Which means onekind of drug is administered to the patient having patient ID “123456”,and there are nine insulin prescriptions corresponding to differentblood glucose levels.

In the case of a patient having patient ID “135792”, there are twoclassification numbers of “1” and “2”. In other words, two kinds ofdrugs are administered to the patient having patient ID “135792”.

The blood glucose measurement procedure and insulin prescriptionprocedure are generally performed at a predetermined time after thepatient having meal. Further, the blood glucose measurement procedureand insulin prescription procedure may also be performed at apredetermined time before the patient having meal. The blood glucosemeasurement procedure and insulin prescription procedure arecollectively performed for a plurality of patients at a predeterminedtime.

The work unit of the blood glucose measurement procedure and/or insulinprescription procedure collectively performed for a plurality ofpatients at a predetermined time is “round”. For example, the expressionof “one round in 30 minutes after breakfast” and the like are used inpractice.

In order to prevent mistake in the blood glucose measurement procedure,the insulin prescription procedure and the like, the measurement datamanagement device 104 only transmits data for performing one round tothe blood glucose meter 102.

Further, after the round is completed, the measurement/prescriptionresults table 1408 is transmitted from the blood glucose meter 102 tothe measurement data management device 104 as soon as the blood glucosemeter 102 is mounted on the cradle 103. Upon receiving themeasurement/prescription results table 1408, the measurement datamanagement device 104 records the measurement/prescription results table1408 in a patient history table (not shown in the drawings) insidethereof.

Other tables than the measurement/prescription table 1602, themeasurement/prescription results table 1408 and the prescriptioninformation table 1502 shown in FIGS. 16A, 16B and 16C will be brieflydescribed below.

The patient table 1109 is a table formed by pairing the “PATIENT ID”field with a “PATIENT NAME” field.

The user table 1113 is a table formed by pairing the “USER ID” fieldwith a “USER NAME” field. Incidentally, since the user who performs themeasurement does not have to be a nurse, but may also be a doctor, thename of “user” is used in the table.

The tip lot table 1117 is a table formed by pairing a “LOT NUMBER OFMEASURING TIP 212” field with a “VALIDITY DATE” field.

The tables described above may be any format as long as the fields andthe records can be clearly recognized. In the case of the blood glucosemeter 102 according to the present embodiment, since data amount storedin the nonvolatile storage 614 is small, the tables may also be textfiles such as comma-delimited files or the like.

[Operation]

Next, the operation of the blood glucose meter 102 will be describedbelow.

FIG. 17 is a state transition diagram showing screen transition of thedisplay unit 615 (LCD 203) of the blood glucose meter 102.

FIG. 18, FIG. 19, FIG. 20 and FIG. 21 are partly enlarged views of thestate transition diagram shown in FIG. 17.

FIGS. 22A, 22B, 22C, 23D, 23E, 23F, 24G, 24H, 24I 24J, 25K, 25L, 25M,25N, 26O, 26P, 26Q, 27R and 27S are schematic views showing nurse'sworkflow and attendant screen transition of the display unit 615 of theblood glucose meter 102.

FIG. 28 is a flowchart showing the flow of overall operation of theblood glucose meter 102.

FIGS. 29 and 30 are flowcharts showing the flow overall measurementprocess of the blood glucose meter 102.

FIGS. 31 and 32 are flowcharts showing the flow of a patient ID scanningprocess.

FIGS. 33 and 34 are flowcharts showing the flow of a user ID scanningprocess.

FIGS. 35 and 36 are flowcharts showing the flow of a tip lot scanningprocess.

FIG. 37 is a flowchart showing the flow of a tip attaching process.

FIG. 38 is a flowchart showing the flow of a measurement executionprocess.

FIGS. 39 and 40 are flowcharts showing the flow of a prescriptiondisplay process.

[Screen Transition]

The screen transition of the display unit 615 of the blood glucose meter102 will be described below with reference to FIG. 17 and FIG. 18.

When the nurse presses the power switch 104 of the blood glucose meter102, an initial screen page P1701 will be displayed on the display unit615.

On the initial screen page P1701, selection can be performed by theCursor keys 205 from three items of “PATIENT MEASUREMENT”, “QC CHECK”and “SYSTEM SETUP”.

When selecting the “QC CHECK” with the Cursor keys 205 and pressing theEnter key 206, a QC check screen page P1702 will be displayed on thedisplay unit 615. Thereafter, the process proceeds to a check procedure,and the details of the check procedure are omitted here.

When selecting the “SYSTEM SETUP” with the Cursor keys 205 and pressingthe Enter key 206, a system setup screen page P1703 will be displayed onthe display unit 615. Thereafter, the process proceeds to a system setupprocedure, and the details of the system setup procedure are omittedhere.

On the initial screen page P1701, when selecting the “PATIENTMEASUREMENT” with the Cursor keys 205 and pressing the Enter key 206,the microcomputer will function as the measurement condition checksection 1002.

First, the control section 1128 causes the QC check section 1103 tofunction, and thereby a QC check process is performed in Step S1751. TheQC check section 1103 compares the QC check record with the current dateand time obtained from the calendar clock 607 to judge, with the judgingsection 1106, whether or not the QC check has been performed within thepredetermined date interval value.

As the judgment result, if it is concluded that the duration from thedate when the last QC check was performed has exceeded the predetermineddate interval value, a QC warning screen page P1704 will be displayed onthe display unit 615 by the control section 1128.

Only the item of “QC CHECK” is displayed on the QC warning screen pageP1704, and only operation of the Enter key 206 can be received. It iscompelled to change the screen from the QC warning screen page P1704 tothe QC check screen page P1702 by operating the Enter key 206.

In the QC check process performed in Step S1751, based on the judgmentresult, if it is concluded that the duration from the date when the lastQC check was performed does not exceed the predetermined date intervalvalue, the control section 1128 will cause the patient ID readingsection 1107 to function, and thereby a patient measurement screen pageP1705 will be displayed on the display unit 615 by the control section1128.

On the patient measurement screen page P1705, selection can be performedby the Cursor keys 205 from three items of “MEASURE”, “DATA” and“RETURN”.

When selecting the “DATA” with the Cursor keys 205 and pressing theEnter key 206, a data screen page P1706 will be displayed on the displayunit 615 by the control section 1128. Thereafter, the process proceedsto a past data display procedure, and the details of the past datadisplay procedure are omitted here.

When selecting the “RETURN” with the Cursor keys 205 and pressing theEnter key 206, the screen will return to the initial screen page P1701.

When selecting the “MEASURE” with the Cursor keys 205 and pressing theEnter key 206, a patient ID scanning screen page P1707 will be displayedon the display unit 615 by the control section 1128.

On the patient ID scanning screen page P1707, only a “RETURN” item canbe selected. At this time, when pressing the Bar-code key 207, under thecontrol of the control section 1128, the red laser diode 622 of thebar-code reader 208 emits light, and the bar-code reader 208 is broughtinto a state capable of performing a bar-code read operation through thephototransistor 623.

If the bar-code reader 208 has successfully read the bar-code, the readbar-code data outputted by the bar-code reader 208 will be once storedin the patient ID variable 1108, and the search section 1110 will searchto see whether or not the data has been registered in the patient table1109 stored in the nonvolatile storage 614.

If the data has not been registered, an “UNREGISTERED” screen page P1708will be displayed on the display unit 615 by the control section 1128.On the “UNREGISTERED” screen page P1708, “OK” is the only item possibleto be selected, therefore only operation of the Enter key 206 can bereceived as operation of the operating section 608. On such screen page,when pressing the Enter key 206, the screen of the display unit 615 willreturn to the patient ID scanning screen page P1707.

If the data has been registered, a patient name display screen pageP1712 will be displayed on the display unit 615 by the control section1128.

If the bar-code has not been successfully read, a read error screen pageP1709 will be displayed on the display unit 615 by the control section1128 until the error has been repeated two times. Only “RETRY”, asselection item, is displayed on this screen page, and only the Enter key206 can be received. On such screen page, when pressing the Enter key206, the screen of the display unit 615 will return to the patient IDscanning screen page P1707.

In the case where the bar-code has not been successfully read, if theerror is repeated three or more times, a read error screen page P1710will be displayed on the display unit 615 by the control section 1128.

As selection item, an item “SELECT FROM LIST” as well as the item“RETRY” are played on such screen page.

When selecting the “RETRY” and pressing the Enter key 206, the screen ofthe display unit 615 will return to the patient ID scanning screen pageP1707.

When selecting the “SELECT FROM LIST” and pressing the Enter key 206, apatient list screen page P1711 will be displayed on the display unit 615by the control section 1128.

On the patient list screen page P1711, a list of patient names andpatient IDs from the patient table 1109 stored in the nonvolatilestorage 614 is displayed. When selecting a patient ID with the Cursorkeys 205 and pressing the Enter key 206, the patient name display screenpage P1712 will be displayed on the display unit 615 by the controlsection 1128.

As timing for displaying the “SELECT FROM LIST”, the number of therepeating times of the read error is not particularly limited, andpreferable number of the repeating times is two to four. Further, otherconditions may be added such as long-pressing the Enter key 206.

When the patient name display screen page P1712 is displayed on thedisplay unit 615, the patient ID read by the bar-code reader 208 orselected on the patient list screen page P1711 is stored in the patientID variable 1108.

On the patient name display screen page P1712, selection can beperformed by the Cursor keys 205 from two items of “OK” and “RETRY”.

When selecting the “RETRY” with the Cursor keys 205 and pressing theEnter key 206, the screen of the display unit 615 will return to thepatient ID scanning screen page P1707.

When selecting the “OK” with the Cursor keys 205 and pressing the Enterkey 206, the control section 1128 will cause the user ID reading section1111 to operate, and thereby a user ID scanning screen page P1713 shownin FIG. 19 will be displayed on the display unit 615 by the controlsection 1128.

The screen transition of the display unit 615 of the blood glucose meter102 after FIG. 18 will be described below with reference to FIG. 17 andFIG. 19.

On the user ID scanning screen page P1713, only a “RETURN” item can beselected. At this time, when pressing the Bar-code key 207, under thecontrol of the control section 1128, the red laser diode 622 of thebar-code reader 208 emits light, and the bar-code reader 208 is broughtinto a state capable of performing a bar-code read operation.

If the bar-code reader 208 has successfully read the bar-code, the readbar-code data will be once stored in the user ID variable 1112, and thesearch section 1114 will search to see whether or not the data has beenregistered in the user table 1113 stored in the nonvolatile storage 614.

If the data has not been registered, an “UNREGISTERED” screen page P1714will be displayed on the display unit 615 by the control section 1128.Only “OK”, as selection item, is displayed on this screen page, and onlythe Enter key 206 is received. When pressing the Enter key 206, thescreen will return to the user ID scanning screen page P1713.

If the data has been registered, a user name display screen page P1718will be displayed on the display unit 615 by the control section 1128.

If the bar-code has not been successfully read, a read error screen pageP1715 will be displayed on the display unit 615 until error has beenrepeated two times. Only “RETRY”, as selection item, is displayed onthis screen page, and only the Enter key 206 is received. When pressingthe Enter key 206, the screen will return to the user ID scanning screenpage P1713.

In the case where the bar-code has not been successfully read, if theerror is repeated three or more times, a read error screen page P1716will be displayed on the display unit 615.

As selection item, an item “SELECT FROM LIST” as well as the item“RETRY” are played on such screen page.

When selecting the “RETRY” and pressing the Enter key 206, the screenwill return to the user ID scanning screen page P1713.

When selecting the “SELECT FROM LIST” and pressing the Enter key 206, auser list screen page P1717 will be displayed on the display unit 615 bythe control section 1128.

On the user list screen page P1717, a list of user names and user IDsfrom the user table 1113 in the nonvolatile storage 614 is displayed.When selecting a user ID with the Cursor keys 205 and pressing the Enterkey 206, the user name display screen page P1718 will be displayed onthe display unit 615.

As timing for displaying the “SELECT FROM LIST”, the number of therepeating times of the read error is not particularly limited, andpreferable number of the repeating times is one to four. Further, otherconditions may be added such as long-pressing the Enter key 206.

When the user name display screen page P1718 is displayed on the displayunit 615, the user ID read by the bar-code reader 208 or selected on theuser list screen page P1717 is stored in the user ID variable 1112.

On the user name display screen page P1718, selection can be performedby the Cursor keys 205 from two items of “OK” and “RETRY”.

When selecting the “RETRY” with the Cursor keys 205 and pressing theEnter key 206, the screen will return to the user ID scanning screenpage P1713.

When selecting the “OK” with the Cursor keys 205 and pressing the Enterkey 206, the verification of the blood glucose measurement flag andinsulin administration confirmation flag of the measurement/prescriptionresults table 1408 will be performed in Step S1752.

In the case where the blood glucose measurement flag is “true” and oneor more insulin administration confirmation flags are “false”, a bloodglucose level display screen page P1739 shown in FIG. 21 will bedisplayed by the control section 1128.

In the case where the state of the blood glucose measurement flag andthe insulin dosage display flag is not the aforesaid combination, a tiplot scanning screen page P1719 will be displayed on the display unit 615by the control section 1128.

Step S1752 is a necessary confirming procedure when collectivelymeasuring the blood glucose for a plurality of patients and thencollectively administering insulin to the plurality of patients havingreceived the blood glucose measurement. In other words, by confirmingthe aforesaid flags, it is possible to confirm whether or not the“collectively measuring” has been performed, instead of individuallymeasuring blood glucose level for each patient and then performinginsulin administration.

On the tip lot scanning screen page P1719, only a “RETURN” item can beselected. At this time, when pressing the Bar-code key 207, the redlaser diode 622 of the bar-code reader 208 will emit light, and thebar-code reader 208 will be brought into a state capable of performing abar-code read operation.

When the bar-code has been successfully read, verification will beperformed to see whether or not the bar-code is the one having beenregistered in the tip lot table 1117 of the nonvolatile storage 614.

If the bar-code has not been registered, an “UNREGISTERED” screen pageP1720 will be displayed on the display unit 615.

Only “OK”, as selection item, is displayed on this screen page, and onlythe Enter key 206 is received. When pressing the Enter key 206, thescreen will return to the tip lot scanning screen page P1719.

If the bar-code has been registered, a tip lot display screen page P1725will be displayed on the display unit 615.

As described above, the tip lots and validity dates of the tip lots arerecorded in the tip lot table 1117.

Even in the case where the bar-code has been successfully read, if it isjudged, by acquiring the current date and time information by thecalendar clock 607, that the lot of the measuring tip 212 has passed thevalidity date, an expiration error screen page P1721 will be displayedon the display unit 615.

Only “OK”, as selection item, is displayed on this screen page, and onlyoperation of the Enter key 206 can be received. When pressing the Enterkey 206, the screen will return to the tip lot scanning screen pageP1719. In other words, it is compelled to attach a measuring tip 212within validity date.

If the bar-code has not been successfully read, a read error screen pageP1722 will be displayed on the display unit 615 by the control section1128 until error has been repeated two times. Only “RETRY”, as selectionitem, is displayed on this screen page, and only operation of the Enterkey 206 can be received. When pressing the Enter key 206, the screenwill return to the tip lot scanning screen page P1719.

In the case where the bar-code has not been successfully read, if theerror is repeated three times, a read error screen page P1723 will bedisplayed on the display unit 615 by the control section 1128.

As selection item, an item “SELECT FROM LIST” as well as the item“RETRY” are played on this screen page.

When selecting the “RETRY” and pressing the Enter key 206, the screenpage will return to the tip lot scanning screen page P1719.

When selecting the “SELECT FROM LIST” and pressing the Enter key 206, atip lot list screen page P1724 will be displayed on the display unit 615by the control section 1128.

On the tip lot list screen page P1724, a list of tip lots from the tiplot table 1117 stored in the nonvolatile storage 614 is displayed. Whenselecting a tip lot with the Cursor keys 205 and pressing the Enter key206, the tip lot display screen page P1725 will be displayed on thedisplay unit 615.

As timing for displaying the “SELECT FROM LIST”, the number of therepeating times of the read error is not particularly limited, andpreferable number of the repeating times is zero to four. Further, otherconditions may be added such as long-pressing the Enter key 206.

When the tip lot display screen page P1725 is displayed on the displayunit 615, the tip lot read by the bar-code reader 208 or selected fromthe tip lot list screen page P1724 is stored in the tip lot variable1116.

On the tip lot display screen page P1725, selection can be performed bythe Cursor keys 205 from two items of “OK” and “RETRY”.

When selecting the “RETRY” with the Cursor keys 205 and pressing theEnter key 206, the screen will return to the tip lot scanning screenpage P1719.

When selecting the “OK” with the Cursor keys 205 and pressing the Enterkey 206, the control section 1128 will cause the temperature checksection 1119 to operate, and thereby temperature check will be performedin Step S1753. Further, if the temperature is within the allowablerange, the control section 1128 will cause the tip attachment checksection 1123 to operate, and thereby a “PLEASE ATTACH A TIP” screen pageP1727 shown in FIG. 20 will be displayed on the display unit 615 by thecontrol section 1128.

If the temperature is not within the allowable range, a temperatureerror screen page P1726 will be displayed on the display unit 615. Whichmeans the ambient temperature is not suitable for performing the bloodglucose measurement. Further, since the blood glucose measurement shouldnot be performed when such screen page appears, only “MENU” can beselected, and it is compelled to return the screen to the initial screenpage P1701.

Incidentally, when the blood glucose meter 102 is not performing theblood glucose measurement operation and insulin dosage displayoperation, the temperature check section 1119 may also periodicallymeasure the temperature at a time interval of one minute, for example.In such case, when it is detected that the temperature is not within theallowable range, it is possible to display an alarm on the display unit615 and prohibit the bar-code reading operation of the patient ID anduser ID, therefore non-productive works can be prevented.

The screen transition of the display unit 615 of the blood glucose meter102 after FIG. 19 will be described below with reference to FIG. 17 andFIG. 20.

On the “PLEASE ATTACH A TIP” screen page P1727, operation of the Cursorkeys 205, Enter key 206 and the like can not be received. The “PLEASEATTACH A TIP” screen page P1727 is displayed to tell that the device isin a state of readiness to detect the normal attachment of the measuringtip 212.

In the case where the “PLEASE ATTACH A TIP” screen page P1727 is beingdisplayed, if a used measuring tip 212 is attached by mistake, the tipattachment detection section 1124 will compare the quantity of thereflected light with the threshold and judge that the measuring tip 212is deemed a used one. Upon receiving such judgment, the control section1128 displays a defective tip screen page P1728 on the display unit 615.Only “OK”, as selection item, is displayed on this screen page, and thescreen returns to the tip lot scanning screen page P1719.

On the “PLEASE ATTACH A TIP” screen page P1727, if a new measuring tip212 is attached, the tip attachment detection section 1124 will detectthat a non-defective product measuring tip 212 has been attached. Uponreceiving the detection result of the tip attachment detection section1124, the control section 1128 functions as the blood glucose measuringsection 1003. As a result, a “MEASURING” screen page P1729 is displayedon the display unit 615 by the control section 1128. This screen pagetells that the device is brought into a state where the opticalmeasuring section 202 is caused to operate, and the optical measuringsection 202 is in a standby state to detect the operation of causing themeasuring tip 212 to soak the blood.

When the blood is soaked into the measuring tip 212, the quantity of thereflected light from the test piece 1127 inside the measuring tip 212will change. When the detection section 1404 detects such change throughthe phototransistor 612 and the A/D converter 613, a “COUNTDOWN” screenpage P1730 will be displayed on the display unit 615 by the controlsection 1128. From this time, the control section 1128 causes a timer tooperate to wait until a predetermined time has elapsed. Thepredetermined time set for the timer is about 12 seconds, and changesaccording to the temperature. The control section 1128 calculates thenecessary change of the predetermined time based on the temperaturemeasured by the thermistor 606.

When the predetermined time has elapsed since the “COUNTDOWN” screenpage P1730 is displayed on the display unit 615, a blood glucose leveldisplay screen page P1732 will be displayed on the display unit 615 bythe control section 1128.

On the blood glucose level display screen page P1732, selection can beperformed by the Cursor keys 205 from two items of “CONFIRM” and “DATA”.

When selecting the “CONFIRM” with the Cursor keys 205 and pressing theEnter key 206, the control section 1128 will confirm all insulinadministration confirmation flags recorded in the records of the patientof the measurement/prescription results table 1408 in Step S1754.

In Step S1754, if all of the insulin administration confirmation flagsare “true”, i.e., if all of the insulin administration processesnecessary for the patient are completed, a blood glucose measurementmenu screen page P1731 will be displayed on the display unit 615 by thecontrol section 1128.

On the blood glucose measurement menu screen page P1731, selection canbe performed by the Cursor keys 205 from two items “REMEASURE” and “NEXTPATIENT”.

When selecting the “REMEASURE” with the Cursor keys 205 and pressing theEnter key 206, the blood glucose measurement flag will be set to “false”in Step S1759, and the screen will return to the patient ID scanningscreen page P1707 (see FIG. 18).

When selecting the “NEXT PATIENT” with the Cursor keys 205 and pressingthe Enter key 206, the blood glucose measurement flag will be set to“true” in Step S1760, and the screen will return to the patient IDscanning screen page P1707.

In Step S1754, when even one of the insulin administration confirmationflags is “false”, i.e., when necessary insulin administration processesfor the patient are not all completed, an insulin administration menuscreen page P1733 will be displayed on the display unit 615 by thecontrol section 1128.

On the insulin administration menu screen page P1733, selection can beperformed by the Cursor keys 205 from three items of “REMEASURE”,“INSULIN” and “NEXT PATIENT”.

When selecting the “REMEASURE” with the Cursor keys 205 and pressing theEnter key 206, the blood glucose measurement flag will be set to “false”in Step S1755, and the screen will return to the patient ID scanningscreen page P1707.

When selecting the “NEXT PATIENT” with the Cursor keys 205 and pressingthe Enter key 206, the blood glucose measurement flag will be set to“true” in Step S1756, and the screen will return to the patient IDscanning screen page P1707.

When selecting the “INSULIN” with the Cursor keys 205 and pressing theEnter key 206, the blood glucose measurement flag will be set to “true”in Step S1756, and the control section 1128 will function as theprescription data display section 804. As a result, an insulin dosagedisplay screen page P1734 shown in FIG. 21 is displayed on the displayunit 615 by the control section 1128.

It can be known by comparing the blood glucose measurement menu screenpage P1731 with the insulin administration menu screen page P1733 that,in the insulin administration menu screen page P1733, an item “INSULIN”can be selected, while in the blood glucose measurement menu screen pageP1731, there is no such item.

With such a configuration, since the all insulin administrationprocesses have been performed for the patient, the accident of executingduplicated administration of insulin can be prevented.

The screen transition of the display unit 615 of the blood glucose meter102 after FIG. 20 will be described below with reference to FIG. 17 andFIG. 21.

On the insulin dosage display screen page P1734, only a “NEXT” item canbe selected. The user such as a nurse or the like views the kind anddosage, i.e., the prescription data, of the insulin displayed on suchscreen page to confirm the kind and dosage of the drug to beadministered to the patient.

On the insulin dosage display screen page P1734, when pressing the Enterkey 206, an administration selection screen page P1735 will be displayedon the display unit 615.

On the administration selection screen page P1735, selection can beperformed by the Cursor keys 205 from two items of “ADMINISTERED” and“UNADMINISTERED”.

When selecting the “ADMINISTERED” with the Cursor keys 205 and pressingthe Enter key 206, the insulin dosage display flag will be set to “true”in Step S1757, and then an “ADMINISTERED” screen page P1736 will bedisplayed on the display unit 615 by the control section 1128.

When selecting the “UNADMINISTERED” with the Cursor keys 205 andpressing the Enter key 206, the insulin dosage display flag will be setto “true” in Step S1757, and thereafter an “UNADMINISTERED” screen pageP1737 will be displayed on the display unit 615 by the control section1128.

Incidentally, the present invention also include a possibleconfiguration in which a selection item “RETURN” is further provided onthe administration selection screen page P1735, and the screen returnsto the insulin dosage display screen page P1734 by selecting the“RETURN”. Further, the present invention also includes another possibleconfiguration in which kind and dosage of the drug to be administered tothe patient is displayed on the administration selection screen pageP1735. By employing the aforesaid selection items, kind and dosage ofthe drug can be reconfirmed when performing insulin administration.

On the “ADMINISTERED” screen page P1736, selection can be performed fromtwo items of “OK” and “RETURN”.

When selecting the “OK” with the Cursor keys 205 and pressing the Enterkey 206, the insulin administration confirmation flag will be set to“true” in Step S1758, and then the process will proceed to Step S1761.

When selecting the “RETURN” with the Cursor keys 205 and pressing theEnter key 206, the screen will return to the administration selectionscreen page P1735.

On the “UNADMINISTERED” screen page P1737, selection can be performedfrom two items of “OK” and “RETURN”.

When selecting the “OK” with the Cursor keys 205 and pressing the Enterkey 206, the process will proceed to Step S1761.

When selecting the “RETURN” with the Cursor keys 205 and pressing theEnter key 206, the screen will return to the administration selectionscreen page P1735.

Note that, unlike the time when the “ADMINISTERED” screen page P1736 isdisplayed, at the time when the “UNADMINISTERED” screen page P1737 isdisplayed, there is no insulin administration confirmation flag set inStep S1758, i.e., the insulin administration confirmation flag keeps in“false” state.

When selecting “OK” on both the “ADMINISTERED” screen page P1736 and“UNADMINISTERED” screen page P1737, the process will proceed to StepS1761.

Similar to Step S1754 (see FIG. 20), in Step S1761, the control section1128 confirms all insulin administration confirmation flags recorded inthe records of the patient of the measurement/prescription results table1408.

In Step S1761, if all of the insulin administration confirmation flagsare “true”, i.e., if all of the insulin administration processesnecessary for the patient are completed, an administration confirmationscreen page P1741 will be displayed on the display unit 615 by thecontrol section 1128.

Only “COMPLETION” can be selected on the administration confirmationscreen page P1741. In other words, only the Enter key 206 can bepressed.

On the administration confirmation screen page P1741, when pressing theEnter key 206, a “NEXT PATIENT” screen page P1738 will be displayed onthe display unit 615 by the control section 1128.

In Step S1761, when even one of the insulin administration confirmationflags is “false”, i.e., when insulin administration processes necessaryfor the patient are not all completed, an administration confirmationscreen page P1740 will be displayed on the display unit 615 by thecontrol section 1128.

On the administration confirmation screen page P1740, selection can beperformed by the Cursor keys 205 from two items of “COMPLETION” and“RETURN”.

When selecting the “COMPLETION” with the Cursor keys 205 and pressingthe Enter key 206, a completion confirmation screen page P1742 will bedisplayed on the display unit 615 by the control section 1128.

When selecting the “RETURN” with the Cursor keys 205 and pressing theEnter key 206, the screen will return to the insulin dosage displayscreen page P1734.

On the completion confirmation screen page P1742, a message is displayedwhich tells that the patient whose prescription is being currentlydisplayed has unadministered drug prescription(s). Further, as selectionitem asking whether the drug(s) should be administered or whether thedrug(s) should be transferred to other patient(s), there are two itemsof “RETURN” and “YES” can be selected.

When selecting the “RETURN” with the Cursor keys 205 and pressing theEnter key 206, the process will proceed to Step S1761. As a result,since there is unadministered drug(s), screen is returned to theadministration confirmation screen page P1740.

When selecting the “YES” with the Cursor keys 205 and pressing the Enterkey 206, a “NEXT PATIENT” screen page P1738 will be displayed on thedisplay unit 615 by the control section 1128.

On the “NEXT PATIENT” screen page P1738, selection can be performed fromthree items of “NEXT PATIENT”, “DATA” and “MENU”.

When selecting the “NEXT PATIENT” with the Cursor keys 205 and pressingthe Enter key 206, the screen will return to the patient ID scanningscreen page P1707 (see FIG. 18).

When selecting the “DATA” with the Cursor keys 205 and pressing theEnter key 206, a data screen page P1706 (see FIG. 18) will be displayedon the display unit 615 by the control section 1128.

When selecting the “MENU” with the Cursor keys 205 and pressing theEnter key 206, the screen will return to the initial screen page P1701(see FIG. 18).

On the blood glucose level display screen page P1739, selection can beperformed by the Cursor keys 205 from two items of “INSULIN” and “DATA”.

When selecting the “INSULIN” with the Cursor keys 205 and pressing theEnter key 206, the insulin dosage display screen page P1734 will bedisplayed on the display unit 615 by the control section 1128.

When selecting the “DATA” with the Cursor keys 205 and pressing theEnter key 206, a data screen page P1706 will be displayed on the displayunit 615 by the control section 1128. After referring to the past bloodglucose measurement history, the screen is returned to blood glucoselevel display screen page P1739 by selecting “RETURN”.

[Workflow and Screen Transition]

Nurse's workflow will be described below with reference to FIG. 22A.

In many cases, insulin administration is performed to hospitalizedpatients before meal. At this time, blood glucose measurement isperformed.

As preparation for performing blood glucose measurement and insulinadministration prescription, a nurse 2202 mounts the blood glucose meter102 on the cradle 103 before the patients having meal. As a result, datacommunication between the measurement data management device 104 and theblood glucose meter 102 is performed through the cradle 103, and themeasurement data management device 104 transfers the patient table 1109,the user table 1113, the tip lot table 1117, the prescriptioninformation table 1502 and the measurement/prescription table 1602 tothe blood glucose meter 102.

However, it is assumed that the blood glucose meter 102 according to thepresent embodiment is in a state where the measurement/prescriptionresults table 1408 left in the blood glucose meter 102 is deleted beforeperforming the blood glucose measurement process and insulinadministration prescription process. To make sure that such procedure isreliably performed, the operation of previously mounting the bloodglucose meter 102 on the cradle 103 must be performed before performingthe blood glucose measurement process and insulin administrationprescription process. The state where the measurement/prescriptionresults table 1408 is deleted represents the state where the bloodglucose meter 102 is ready for performing measurement.

Description of the nurse's workflow will be continued below withreference to FIG. 22B.

The nurse 2202 prepares the blood glucose meter 102, measuring tips 2203and insulin syringes 2204 and goes from the nurse station to thehospital ward, wherein the number of the measuring tips 2203 and thenumber of the insulin syringes 2204 are equal to or more than the numberof the patients.

Description of the nurse's workflow will be continued below withreference to FIG. 22C.

In FIG. 22C, upon reaching the bed of a patient 2205, the nurse 2202starts the blood glucose measurement process with the blood glucosemeter 102.

Description of the nurse's workflow will be continued below withreference to FIG. 23D.

The nurse 2202 operates the blood glucose meter 102 to display thepatient ID scanning screen page P1707 on the LCD 203. Further, the nurse2202 presses the Bar-code key 207 to cause the bar-code reader 208 toscan a patient ID 2306, which is a bar-code, of the patient 2205.

If bar-code reading is successful, the patient name display screen pageP1712 will be displayed on the LCD 203.

The nurse 2202 confirms the contents of the display, selects “OK” withthe Cursor keys 205, and presses the Enter key 206. As a result, theuser ID scanning screen page P1713 is displayed on the LCD 203.

Description of the nurse's workflow will be continued below withreference to FIG. 23E.

In the state where the user ID scanning screen page P1713 is beingdisplayed on the LCD 203, the nurse 2202 presses the Bar-code key 207 tocause the bar-code reader 208 to scan a nurse ID 2307, which is abar-code, of the nurse 2202.

If bar-code reading is successful, the user name display screen pageP1718 will be displayed on the LCD 203.

The nurse 2202 confirms the contents of the display, selects “OK” withthe Cursor keys 205, and presses the Enter key 206. As a result, the tiplot scanning screen page P1719 is displayed on the LCD 203.

Description of the nurse's workflow will be continued below withreference to FIG. 23F.

In the state where the tip lot scanning screen page P1719 is beingdisplayed on the LCD 203, the nurse 2202 presses the Bar-code key 207 tocause the bar-code reader 208 to scan a tip lot 2308, which is abar-code, printed on a box 2309 or wrapping of the measuring tip 2203.

If bar-code reading is successful, the tip lot display screen page P1725will be displayed on the LCD 203.

The nurse 2202 confirms the contents of the display, selects “OK” withthe Cursor keys 205, and presses the Enter key 206. As a result, the“PLEASE ATTACH A TIP” screen page P1727 is displayed on the LCD 203.

Description of the nurse's workflow will be continued below withreference to FIG. 24G.

In the state where the “PLEASE ATTACH A TIP” screen page P1727 is beingdisplayed on the LCD 203, the nurse 2202 attaches a measuring tip 2203to the optical measuring section 202 of the blood glucose meter 102. Asa result, the blood glucose meter 102 detects that a new measuring tip2203 is normally attached, and the “MEASURING” screen page P1729 isdisplayed on the LCD 203.

Description of the nurse's workflow will be continued below withreference to FIG. 24H.

The nurse 2202 punctures the lateral face of a fingertip 2402 of thepatient 2205 with a puncture tool 2403. As a result, a tiny hole ispunctured in the lateral face of fingertip 2402 by a needle, and bloodis exuded from the hole.

Description of the nurse's workflow will be continued below withreference to FIG. 24I.

The nurse 2202 soaks the blood exuded from the fingertip 2402 of thepatient 2205 into the measuring tip 2203 of the blood glucose meter 102.As a result, by soaking the blood into the test piece 1127 inside themeasuring tip 2203, the blood glucose meter 102 detects the quantity ofthe light reflected from the test piece 1127 and displays the“COUNTDOWN” screen page P1730 on the LCD 203.

When a predetermined time has elapsed since the “COUNTDOWN” screen pageP1730 is displayed, the blood glucose measurement is performed, and theblood glucose level display screen page P1732 is displayed on the LCD203.

The nurse 2202 confirms the contents of the display, selects “CONFIRM”with the Cursor keys 205, and presses the Enter key 206. As a result, inthe case where there is unadministered drug(s), the insulinadministration menu screen page P1733 is displayed on the LCD 203.

Description of the nurse's workflow will be continued below withreference to FIG. 24J.

In the state where the insulin administration menu screen page P1733 isbeing displayed on the LCD 203, the nurse 2202 selects “INSULIN” withthe Cursor keys 205, and presses the Enter key 206.

As a result, the blood glucose measurement flag is set to “true”, andthe insulin dosage display screen page P1734 is displayed on the LCD 203by the control section 1128 of the blood glucose meter 102.

Description of the nurse's workflow will be continued below withreference to FIG. 25K.

Following the content of the insulin dosage display screen page P1734displayed on the LCD 203, the nurse 2202 administers insulin to thepatient 2205 using the insulin syringe 2204.

Description of the nurse's workflow will be continued below withreference to FIG. 25L.

After completing the insulin administration process, the nurse 2202presses the Enter key 206.

As a result, the insulin dosage display flag is set to “true”, and theadministration selection screen page P1735 is displayed on the LCD 203by the control section 1128 of the blood glucose meter 102.

Description of the nurse's workflow will be continued below withreference to FIG. 25M.

In the state where the administration selection screen page P1735 isbeing displayed on the LCD 203, the nurse 2202 selects “ADMINISTERED”with the Cursor keys 205, and presses the Enter key 206.

As a result, the insulin administration confirmation flag is set to“true”, and the “ADMINISTERED” screen page P1736 is displayed on the LCD203 by the control section 1128 of the blood glucose meter 102.

Description of the nurse's workflow will be continued below withreference to FIG. 25N.

In the state where the “ADMINISTERED” screen page P1736 is beingdisplayed on the LCD 203, the nurse 2202 selects “OK” with the Cursorkeys 205, and presses the Enter key 206.

Thereafter, in the case where there is unadministered drug(s), theadministration confirmation screen page P1740 is displayed on the LCD203, and further, after the screen has proceeded to the completionconfirmation screen page P1742, the “NEXT PATIENT” screen page P1738 isdisplayed. Further, in the case where there is no unadministered drug,after the screen has proceeded to the administration confirmation screenpage P1741, the “NEXT PATIENT” screen page P1738 is displayed.

Description of the nurse's workflow will be continued below withreference to FIG. 26O.

In the state where the “NEXT PATIENT” screen page P1738 is beingdisplayed on the LCD 203, the nurse 2202 selects “NEXT PATIENT” with theCursor keys 205, and presses the Enter key 206.

As a result, the content displayed on the LCD 203 returns to the patientID scanning screen page P1707 shown in FIG. 23D to continue measurementprocess for the next patient.

Description of the nurse's workflow will be continued below withreference to FIG. 26P.

After completing the blood glucose measurement process and insulinadministration process for the patient 2205 in the hospital ward, thenurse 2202 returns to the nurse station.

Description of the nurse's workflow will be continued below withreference to FIG. 26Q.

After returning to the nurse station from the hospital ward, the nurse2202 mounts the blood glucose meter 102 on the cradle 103. As a result,the measurement data management device 104 recognizes the connectionwith the blood glucose meter 102 through the cradle 103, and requiresthe blood glucose meter 102 to transmit the measurement/prescriptionresults table 1408.

Following the instruction from the measurement data management device104, the blood glucose meter 102 transmits the measurement/prescriptionresults table 1408 to the measurement data management device 104.

After normally receiving the measurement/prescription results table1408, the measurement data management device 104 notifies the bloodglucose meter 102 that the measurement/prescription results table 1408has been normally received.

After receiving the report that “the measurement/prescription resultstable 1408 has been normally received” from the measurement datamanagement device 104, the blood glucose meter 102 deletes themeasurement/prescription results table 1408 stored in the nonvolatilestorage 614.

Description of the nurse's workflow will be continued below withreference to FIG. 27R.

Even if the nurse 2202 is going to administer insulin again to the samepatient by mistake, the insulin dosage display flag has been set to“true” and additionally recorded in the measurement/prescription resultstable 1408 when the administration selection screen page P1735 wasdisplayed for administering insulin last time. The matter that theinsulin dosage display flag has been set to “true” is detected by thecontrol section 1128, and when performing blood glucose measurement, theblood glucose measurement menu screen page P1731 will be displayed onthe LCD 203, and there is no item of “INSULIN” for being selected.

Thus, it is possible to prevent the accident of duplicatedadministration of insulin.

Description of the nurse's workflow will be continued below withreference to FIG. 27S.

After completing the blood glucose measurement of the patient 2205, inthe state where the insulin administration menu screen page P1733 isdisplayed (see FIG. 24J), the nurse 2202 selects “NEXT PATIENT” with theCursor keys 205, and presses the Enter key 206, so that the processproceeds to the blood glucose measurement process for another patient2710. At this time, “true” is recorded in the “BLOOD GLUCOSE MEASUREMENTFLAG” field of the record of the patient 2205 of themeasurement/prescription results table 1408. Thus, when scanning thepatient ID of the patient 2205 and the nurse ID of the nurse 2202 forinsulin prescription, the blood glucose level of the patient 2205measured last time is read out from the measurement/prescription resultstable 1408 and displayed on the blood glucose level display screen pageP1739.

Thus, the operation of performing “collective measurement” and thenperforming “collective administration” on a plurality of patients can becarried out safely and rapidly.

[Flow of Operation]

FIG. 28 is a flowchart showing the flow of overall operation of theblood glucose meter 102.

When the nurse 2202 presses the power switch 104 of the blood glucosemeter 102 (S2801), the program stored in the ROM 603 is read by the CPU502 to perform a predetermined initializing process (S2802), and thenthe initial screen page P1701 is displayed (S2803) to wait key operation(S2804).

If the item selected by the Enter key 206 is “PATIENT MEASUREMENT” (YESin Step S2805), the measurement process will be performed (S2806), and aseries of operation will be terminated (S2810).

If the item selected by the Enter key 206 is “QC CHECK” (YES in StepS2807), the QC check will be performed (S2808), and a series ofoperation will be terminated (S2810).

If the item selected by the Enter key 206 is “SYSTEM SETUP” (NO in StepS2807), a setting process will be performed (S2809), and a series ofoperation will be terminated (S2810).

Note that, during the period while the power is turned on and the bloodglucose meter 102 is not mounted on the cradle 103, the whole process isa loop process repeatedly performed from Step S2803, as indicated by adotted arrow shown in FIG. 28.

FIGS. 29 and 30 are flowcharts showing the flow of the measurementprocess of the blood glucose meter 102. The flow of FIGS. 29 and 30corresponds to Step S2806.

The flow of the measurement process of the blood glucose meter 102 willbe described below with reference to FIG. 29.

When the process is started (S2901), the microcomputer operates as themeasurement condition check section 1002. The control section 1128causes the QC check section 1103 to operate so as to perform QC check(S2902).

Based on result of the QC check performed by the QC check section 1103,if the judging section 1106 judges that the QC check has not beenperformed within the predetermined date interval value 1104 (NO in StepS2903), the control section 1128 will display the QC warning screen pageP1704 on the display unit 615 (S2904). The operation of the Enter key206 will be waited (S2905), and if the Enter key 206 is operated, the QCcheck will be performed (S2906), and the process will be terminated(S2907).

In other words, Steps S2902 and S2903 are equal to Step S1751 of FIG.18.

Based on result of the QC check performed by the QC check section 1103,if the judging section 1106 judges that the QC check has been performedwithin the predetermined date interval value 1104 (YES in Step S2903),the control section 1128 will cause the patient ID reading section 1107to operate, the switch 1116 will be connected to the patient IDvariable, the read information of the bar-code reader 208 will be storedin the patient ID variable 1108, and then the patient measurement screenpage P1705 will be displayed (S2908). Thereafter, key operation iswaited (S2909).

If the item selected by the Enter key 206 is “MEASURE” (YES in StepS2910), the control section 1128 will perform patient ID scanningprocess (S2914).

If the item selected by the Enter key 206 is “DATA” (YES in Step S2911),the control section 1128 will perform a data display process (S2912),and the screen will be returned to the patient measurement screen pageP1705 (S2908).

If the item selected by the Enter key 206 is “RETURN” (NO in StepS2911), the control section 1128 will terminate a series of process(S2913), and the screen will return to the initial screen page P1701(S2803).

During the patient ID scanning process (S2914), if the item selected byoperating the Enter key 206 is “OK” (YES in Step S2915), the controlsection 1128 will perform user ID scanning process (S2916).

During the user ID scanning process (S2916), if the item selected byoperating the Enter key 206 is “OK” (YES in Step S2917), the controlsection 1128 will verify the blood glucose measurement flag and theinsulin dosage display flag (S2918).

In the case where the blood glucose measurement flag is “true” and theinsulin dosage display flag is “false” (YES in S2918), the controlsection 1128 will display the blood glucose level display screen pageP1739 on the display unit 615 (S2919). Further, key operation is waited(S2920).

If the item selected by the Enter key 206 is “INSULIN” (YES in StepS2921), the process will proceed to a prescription information tablesearch process (S3909) and a prescription display process (S3910) in theflow of the prescription display process shown in FIG. 39.

If the item selected by the Enter key 206 is “DATA” (NO in Step S2921),the process will proceed to the data display process (S2912).

In Step S2918, if the state of the blood glucose measurement flag andthe insulin dosage display flag is not a combination of “the bloodglucose measurement flag is ‘true’ and the insulin dosage display flagis ‘false’” (NO in Step S2918), the tip lot scanning process will beperformed (S2922).

In other words, Step S2918 is just Step S1752 of FIG. 19.

The flow of the measurement process of the blood glucose meter 102following FIG. 29 will be described below with reference to FIG. 30.

Within the tip lot scanning process (S2922), if the item selected byoperating the Enter key 206 is “OK” (YES in Step S2923), temperaturecheck will be performed by the temperature check section 1119.

Based on the result of temperature check, if the temperature is notwithin an operation-guaranteed temperature range (NO in Step S3025), thecontrol section 1128 will display the temperature error screen pageP1726 on the display unit 615 (S3026) to wait key operation (S3027), andthen process will be terminated (S3028).

In other words, Steps S3024 and S3025 are equal to Step S1753 of FIG.19.

Based on the result of temperature check performed by the temperaturecheck section 1119, if the temperature is within an operation-guaranteedtemperature range (YES in Step S3025), tip attaching process will beperformed (S3029).

Based on the result of the tip attaching process (S3029), if theattached measuring tip 2203 is a defective product (NO in Step S3030),the defective tip screen page P1728 will be displayed (S3031) to waitkey operation (S3032), and the process will return to the tip lotscanning process (S2922).

Based on the result of the tip attaching process (S3029), if theattached measuring tip 2203 is a non-defective product (YES in StepS3030), the microcomputer will operate as the blood glucose measuringsection 1003. Further, a measurement execution process will be performed(S3033).

After performing the measurement execution process (S3033), the bloodglucose level display screen page P1732 is displayed (S3034) to wait keyoperation (S3035).

If the item selected by operating the Enter key 206 is “DATA” (NO inStep S3036), the process will proceed to the data display process(S2912).

If the item selected by operating the Enter key 206 is “CONFIRM” (YES inStep S3036), the control section 1128 will confirm all insulinadministration confirmation flags recorded in the record of the patientin the measurement/prescription results table 1408.

In Step S3037, when even one of the insulin administration confirmationflags is “false”, i.e., when insulin administration processes necessaryfor the patient are not all completed, the process will proceed toprescription display process (S3038).

At the end of the prescription display process (S3038), if the itemselected by operating the Enter key 206 (Step S3914 of FIG. 39) is “NEXTPATIENT” (YES in Step S3039), the process will return to patient IDscanning process (S2914).

At the end of the prescription display process (S3038), if the itemselected by operating the Enter key 206 (Step S3914 of FIG. 39) is“DATA” (NO in Step S3039 and YES in Step S3040), the process willproceed to data display process (S2912).

At the end of the prescription display process (S3038), if the itemselected by operating the Enter key 206 (Step S3914 of FIG. 39) is“MENU” (NO in Step S3039 and NO in Step S3040), the process will beterminated (S3041).

In Step S3037, if all of the insulin administration confirmation flagsare “true”, i.e., if all of the insulin administration processesnecessary for the patient are completed (NO in Step S3037), the bloodglucose measurement menu screen page P1731 will be displayed on thedisplay unit (S3042) to wait key operation (S3043).

If the item selected by the Enter key 206 is “REMEASURE” (YES in StepS3044), the blood glucose measurement flag will be set to “false”(S3045), and the process will return to the patient ID scanning process(S2914).

If the item selected by the Enter key 206 is “NEXT PATIENT” (NO in StepS3044), the blood glucose measurement flag will be set to “true”(S3046), and the process will return to the patient ID scanning process(S2914).

FIGS. 31 and 32 are flowcharts showing the flow of the patient IDscanning process. The flow of FIGS. 31 and 32 corresponds to Step S2914of FIG. 29.

The flow of the patient ID scanning process of the blood glucose meter102 will be described below with reference to FIG. 31.

When the process is started (S2901), the patient ID scanning screen pageP1707 is displayed (S3102) to wait bar-code or key operation (S3103).

If the item selected by operating the Enter key 206 is “RETURN” (YES inStep S3104), the process will be terminated (S3105). Further, thecontent of the selection item at this time (“RETURN”) will be reflectedby the judgment of Step S2915 (NO in Step S2915), and the screen will bereturned to the patient measurement screen page P1705 (S2908).

If the result of the bar-code reader or key operation is not “RETURN”(NO in Step S3104), whether or not the bar-code has been read will beverified (S3106). If the bar-code has been normally read (YES in StepS3106), the read data deemed to be the patient ID will be compared withthe patient table 1109 (S3107). As a result, if the read data does notexist in the patient table 1109 (NO in Step S3108), the “UNREGISTERED”screen page P1708 will be displayed (S3109) to wait key operation(S3110), and the screen will be returned to the patient ID scanningscreen page P1707 (S3102).

In Step S3107, if the read data exists in the patient table 1109 (YES inStep S3108), the patient name display screen page P1712 will bedisplayed (S3111) to wait key operation (S3112).

If the item selected by operating the Enter key 206 is “OK” (YES in StepS3113), the process will be terminated (S3114). Further, the content ofthe selection item at this time (“OK”) will be reflected by the judgmentof Step S2915 (YES in Step S2915), and the process will proceed to userID scanning process (S2916).

The flow of the patient ID scanning process of the blood glucose meter102 will be further described below with reference to FIG. 32.

In Step S3106, if the bar-code has not been normally read (NO in StepS3106), an error counter inside the control section 1128 will beincremented (S3215).

Next, whether or not the value of the error counter exceeds two isverified (S3216). If the value of the error counter does not exceed two(NO in Step S3216), the read error screen page P1709 will be displayed(S3217) to wait key operation (S3218), and the screen will be returnedto the patient ID scanning screen page P1707 (S3102).

If the value of the error counter exceeds two (YES in Step S3216), theread error screen page P1710 will be displayed (S3219) to wait keyoperation (S3220).

If the item selected by operating the Enter key 206 in Step S3220 is“RETRY” (NO in Step S3221) instead of “SELECT FROM LIST”, the screenwill be returned to the patient ID scanning screen page P1707 (S3102).

If the item selected by operating the Enter key 206 in Step S3220 is“SELECT FROM LIST” (YES in Step S3221), the patient list screen pageP1711 will be displayed (S3222) to wait key selecting operation (S3223).Further, the patient ID selected by the user is determined as thepatient ID to be subjected to the blood glucose measurement (S3224), andthe process is returned to Step S3111.

FIGS. 33 and 34 are flowcharts showing the flow of the user ID scanningprocess. The flow of FIGS. 33 and 34 corresponds to Step S2916 of FIG.29.

The flow of the user ID scanning process of the blood glucose meter 102will be described below with reference to FIG. 33.

When the process is started (S3301), the user ID scanning screen pageP1713 is displayed (S3302) to wait bar-code or key operation (S3303).

If the item selected by operating the Enter key 206 is “RETURN” (YES inStep S3304), the process will be terminated (S3305). Further, thecontent of the selection item at this time (“RETURN”) will be reflectedby the judgment of Step S2917 (NO in Step S2917), and the screen will bereturned to the patient measurement screen page P1705 (S2908).

If the result of the bar-code reader or key operation is not “RETURN”(NO in Step S3304), whether or not the bar-code has been read will beverified (S3306). If the bar-code has been normally read (YES in StepS3306), the read data deemed to be the patient ID will be compared withthe user table (S3307). As a result, if the read data does not exist inthe user table (NO in Step S3308), the “UNREGISTERED” screen page P1714will be displayed (S3309) to wait key operation (S3310), and the screenis returned to the user ID scanning screen page P1713 (S3302).

In Step S3307, if the read data exists in the user table (YES in StepS3308), the user name display screen page P1718 will be displayed(S3311) to wait key operation (S3312).

If the item selected by operating the Enter key 206 is “OK” (YES in StepS3313), the process will be terminated (S3314). Further, the content ofthe selection item at this time (“OK”) will be reflected by the judgmentof Step S2917 (YES in Step S2917), and the process will proceed to StepS2918.

The flow of the user ID scanning process of the blood glucose meter 102will be further described below with reference to FIG. 34.

In Step S3306, if the bar-code has not been normally read (NO in StepS3306), an error counter inside the control section 1128 will beincremented (S3415).

Next, whether or not the value of the error counter exceeds two isverified (S3416). If the value of the error counter does not exceed two(NO in Step S3416), the read error screen page P1715 will be displayed(S3417) to wait key operation (S3418), and the screen will be returnedto the user ID scanning screen page P1713 (S3302).

If the value of the error counter exceeds two (YES in Step S3416), theread error screen page P1716 will be displayed (S3419) to wait keyoperation (S3420).

If the item selected by operating the Enter key 206 in Step S3420 is“RETRY” (NO in Step S3421) instead of “SELECT FROM LIST”, the screenwill be returned to the user ID scanning screen page P1713 (S3302).

If the item selected by operating the Enter key 206 in Step S3420 is“SELECT FROM LIST” (YES in Step S3421), the user list screen page P1717will be displayed (S3422) to wait key selecting operation (S3423).Further, the user ID selected by the user is determined as the user IDwho is going to perform the blood glucose measurement (S3424), and theprocess is returned to Step S3311.

FIGS. 35 and 36 are flowcharts showing the flow of the tip lot scanningprocess. The flow of FIGS. 35 and 36 corresponds to Step S2922 of FIG.29.

The flow of the tip lot scanning process of the blood glucose meter 102will be described below with reference to FIG. 35.

When the process is started (S3501), the tip lot scanning screen pageP1719 is displayed (S3502) to wait bar-code or key operation (S3503).

If the item selected by operating the Enter key 206 is “RETURN” (YES inStep S3504), the process will be terminated (S3505). Further, thecontent of the selection item at this time (“RETURN”) will be reflectedby the judgment of Step S2923 (NO in Step S2923), and the screen will bereturned to the patient measurement screen page P1705 (S2908).

If the result of the bar-code reader or key operation is not “RETURN”(NO in Step S3504), whether or not the bar-code has been read will beverified (S3506). If the bar-code has been normally read (YES in StepS3606), the read data deemed to be the tip lot will be compared with thetip lot table (S3507). As a result, if the read data does not exist inthe tip lot table (NO in Step S3808), the “UNREGISTERED” screen pageP1720 will be displayed (S3509) to wait key operation (S3510), and thescreen will be returned to the tip lot scanning screen page P1719(S3502).

In Step S3507, if the read data exists in the tip lot table (YES in StepS3508), whether or not the lot is within validity date will be verified(S3511). If validity date is expired (NO in Step S3511), the expirationerror screen page P1721 will be displayed (S3512) to wait key operation(S3510), and the screen will be returned to the tip lot scanning screenpage P1719 (S3502).

If it is judged that the lot is within validity date (YES in StepS3511), the tip lot display screen page P1725 will be displayed (S3513)to wait key operation (S3514).

If the item selected by operating the Enter key 206 is “OK” (YES in StepS3515), the process will be terminated (S3516). Further, the content ofthe selection item at this time (“OK”) will be reflected by the judgmentof Step S2923 (YES in Step S2923), and the process will proceed to StepS3024.

The flow of the tip lot scanning process of the blood glucose meter 102will be further described below with reference to FIG. 36.

In Step S3506, if the bar-code has not been normally read (NO in StepS3506), an error counter inside the control section 1128 will beincremented (S3617).

Next, whether or not the value of the error counter exceeds two isverified (S3618). If the value of the error counter does not exceed two(NO in Step S3618), the read error screen page P1722 will be displayed(S3619) to wait key operation (S3620), and the screen will be returnedto the tip lot scanning screen page P1719 (S3502).

If the value of the error counter exceeds two (YES in Step S3618), theread error screen page P1723 will be displayed (S3621) to wait keyoperation (S3622).

If the item selected by operating the Enter key 206 in Step S3622 is“RETRY” (NO in Step S3622) instead of “SELECT FROM LIST”, the screenwill be returned to the tip lot scanning screen page P1719 (S3502).

If the item selected by operating the Enter key 206 in Step S3622 is“SELECT FROM LIST” (YES in Step S3623), the tip lot list screen pageP1724 will be displayed (S3624) to wait key selecting operation (S3625).Further, the tip lot selected by the user is determined as the lot ofthe measuring tip 2203 to be used to perform the blood glucosemeasurement (S3626), and the process is returned to Step S3513.

FIG. 37 is a flowchart showing the flow of the tip attaching process.The flow of FIG. 37 corresponds to Step S3029 of FIG. 30.

When the process is started (S3701), the control section 1128 displaysthe “PLEASE ATTACH A TIP” screen page P1727 on the display unit 615(S3702) and causes the tip attachment check section 1123 to operate. Thecontrol section 1128 performs on-control of the switch 1126 to cause theD/A converter 611 to convert the adjustment value data 925 into ananalog voltage to drive the driver 610 to control the light emission ofthe light-emitting diode 609. Further, the reflected light from the testpiece 1127 is received by the phototransistor 612, and the reflectedlight measurement is performed (S3703).

The reflected light data inputted to the tip attachment detectionsection 1124 from the phototransistor 612 through the A/D converter 613is continuously polled (S3704). If the phototransistor 612 detects thereflected light (YES in Step S3704), the process will be terminated(S3705).

FIG. 38 is a flowchart showing the flow of the measurement executionprocess. The flow of FIG. 38 corresponds to Step S3033 of FIG. 30.

When the process is started (S3801), the control section 1128 displaysthe “MEASURING” screen page P1729 on the display unit 615 (S3802).

Whether or not there is a change in reflected light data obtained fromthe phototransistor 612 is polled (S3803).

If a change in quantity of the reflected light is detected (YES in StepS3803), a timer inside the control section 1128 is started (S3804), andthe “COUNTDOWN” screen page P1730 is displayed on the display unit 615(S3805).

When a preset time (12 seconds ±α) has elapsed (YES in Step S3806), thequantity of the reflected light will be measured, the blood glucoselevel will be calculated based on the quantity of the reflected light(S3807), and the process will be terminated (S3808).

FIGS. 39 and 40 are flowcharts showing the flow of the prescriptiondisplay process. The flow of FIGS. 39 and 40 corresponds to Step S3038of FIG. 30.

The flow of the prescription display process of the blood glucose meter102 will be described below with reference to FIG. 39.

When the process is started (S3901), the insulin administration menuscreen page P1733 is displayed (S3902) to wait key operation (S3903).

If the item selected by operating the Enter key 206 in Step S3903 is“INSULIN” (YES in Step S3904), the blood glucose measurement flag willbe set to “true” (S3908).

If the item selected by operating the Enter key 206 in Step S3903 is“REMEASURE” (YES in Step S3905), the blood glucose measurement flag willbe set to “false” (S3906). If the item selected by operating the Enterkey 206 in Step S3903 is “NEXT PATIENT” (NO in Step S3905), the bloodglucose measurement flag will be set to “true” (S3907).

After the process of Steps S3906 and S3907, the process is returned tothe patient ID scanning process (S2914).

After the process of Step S3908, the control section 1128 controls thesearch section 1503 to search the prescription information table 1502(S3909), and the insulin dosage display screen page P1734 is displayed(S3910) to wait key operation (S3911).

If the Enter key 206 is pressed by the user, the administrationselection screen page P1735 will be displayed (S3912), and the insulindosage display flag will be set to “true” (S3913) to wait key operation(S3914).

The flow of the prescription display process of the blood glucose meter102 will be further described below with reference to FIG. 40.

If the item selected by operating the Enter key 206 in Step S3914 is“ADMINISTERED” (YES in Step S4015), the “ADMINISTERED” screen page P1736will be displayed (S4016) to wait key operation (S4017).

If the item selected by operating the Enter key 206 in Step S4017 is“RETURN” (NO in Step S4018), the administration selection screen pageP1735 will be displayed again (S3912), and the insulin dosage displayflag regarding the currently displayed drug will be set to “true”(S3913) to wait key operation (S3914).

If the item selected by operating the Enter key 206 in Step S4017 is“OK” (YES in Step S4018), the insulin dosage display flag regarding thecurrently displayed drug will be set to “true” (S4019), and the processwill proceed to Step S4020.

If the item selected by operating the Enter key 206 in Step S3914 is“UNADMINISTERED” (NO in Step S4015), the “UNADMINISTERED” screen pageP1737 will be displayed (S4021) to wait key operation (S4022).

If the item selected by operating the Enter key 206 in Step S4022 is“RETURN” (NO in Step S4023), the administration selection screen pageP1735 will be displayed again (S3912), and the insulin dosage displayflag regarding the currently displayed drug will be set to “true”(S3913) to wait key operation (S3914).

If the item selected by operating the Enter key 206 in Step S4022 is“OK” (YES in Step S4023), the process will proceed to Step S4020. Inother words, the insulin dosage display flag regarding the currentlydisplayed drug remains “false”.

After Steps S4019 and S4023, the control section 1128 confirms theprescription of the present patient. The control section 1128 confirmsall records in the “INSULIN ADMINISTRATION INFORMATION” field in therecord of the patient. In other words, the control section 1128 confirmsthe insulin administration confirmation flags regarding allprescriptions. As a result, when even one of the “INSULIN ADMINISTRATIONCONFIRMATION FLAG” field is “false”, i.e., when even one drugunadministered to the patient exists (YES in Step S4020), theadministration confirmation screen page P1740 will be displayed (S4024)to wait key operation (S4025).

If the item selected by operating the Enter key 206 in Step S4025 is“RETURN” (NO in Step S4026), the prescription information table 1502will be searched again (S3909), and the insulin dosage display screenpage P1734 will be displayed (S3910) to wait key operation (S3911).

If the item selected by operating the Enter key 206 in Step S4025 is“OK” (YES in Step S4026), the completion confirmation screen page P1742will be displayed (S4027) to wait key operation (S4028).

If the item selected by operating the Enter key 206 in Step S4028 is“RETURN” (NO in Step S4029), the process will be returned to Step S4020.

If the item selected by operating the Enter key 206 in Step S4028 is“YES” (YES in Step S4029), the “NEXT PATIENT” screen page P1738 will bedisplayed (S4030), and the process will be terminated (S4031).

In Step S4020, the control section 1128 confirms all records in the“INSULIN ADMINISTRATION INFORMATION” field in the record of the patient,namely the control section 1128 confirms the insulin administrationconfirmation flags regarding all prescriptions. Based on the result ofthe confirmation performed by the control section 1128, if all “INSULINADMINISTRATION CONFIRMATION FLAG” fields are “true”, namely if all drugsare administered to the patient (NO in Step S4020), the administrationconfirmation screen page P1741 will be displayed (S4032) to wait keyoperation (S4033).

In Step S4033, since “COMPLETION” is the only item possible to beselected, thereafter the “NEXT PATIENT” screen page P1738 is displayed,and the process is terminated.

The present embodiment includes application examples such as thefollowing.

-   (1) In Step S1754 of FIG. 20 and Step S3037 of FIG. 30, the insulin    administration confirmation flags are used as a basis for making a    judgment for preventing duplicated administration of insulin.    Instead of the insulin administration confirmation flag, the insulin    dosage display flag can be used as a basis for making a judgment for    preventing duplicated administration of insulin.

FIG. 41 is a partial view extracted from a screen transition diagrambased on the application example. FIG. 41 corresponds to thesubstitution of Step S1754 of FIG. 20. To be specific, after the“COUNTDOWN” screen page P1730 of FIG. 20 is displayed, the state of theinsulin dosage display flags is confirmed in Step S4154 (instead ofconfirming the insulin administration confirmation flags in Step S1754),and the process proceeds to the blood glucose level display screen pageP1731 or P1733.

FIG. 41 is a partial view extracted from a flowchart based on theapplication example. FIG. 42 corresponds to the substitution of StepS3037 of FIG. 30. To be specific, the state of the insulin dosagedisplay flags is confirmed in Step S4237 (instead of confirming the“true” and “false” of the insulin administration confirmation flags inStep S3037), and the process proceeds to Step P3038 or P3042.

FIG. 43 is a partial view extracted from a screen transition diagrambased on the application example. FIG. 43 corresponds to thesubstitution of Step S1761 of FIG. 21. To be specific, after the“ADMINISTERED” screen page P1736 is displayed and “OK” is selected, orafter the “UNADMINISTERED” screen page P1737 is displayed and “OK” isselected, the state of the insulin dosage display flags is confirmed inStep S4361 (instead of confirming the insulin administrationconfirmation flags in Step S1761), and the process proceeds to any theadministration confirmation screen page P1740 or administrationconfirmation screen page P1741.

FIG. 44 is a partial view extracted from a flowchart based on theapplication example. FIG. 44 corresponds to the substitution of StepS4020 of FIG. 40. To be specific, the state of the insulin dosagedisplay flags is confirmed in Step S4420 (instead of confirming the“true” and “false” of the insulin administration confirmation flags inStep S4020), and the process proceeds to Step P4024 or P4032.

-   (2) By setting the value of the “PRESCRIPTION NUMBER” field of the    measurement/prescription table 1602 for being previously transferred    to the blood glucose meter to “1” so as not to record data in the    record of the patient corresponding to the prescription information    table 1502, it is possible to only perform blood glucose measurement    to the patient.-   (3) The communication method between the blood glucose meter and the    cradle is not limited to IrDA, but can be other communication    methods such as short-distance non-contact electromagnetic induction    using an IC card, Bluetooth (registered trademark), wireless LAN and    the like. Further, there is another possible configuration in which    the cradle is provided with no communication function, and the blood    glucose meter and the personal computer directly communicate with    other via a wireless LAN or the like.-   (4) The configuration of the fields of the prescription information    table 1502 is not limited to the configuration shown in FIG. 16C.

Similar to the “INSULIN ADMINISTRATION INFORMATION” field of themeasurement/prescription results table 1408, if a variable-length“CLASSIFICATION INFORMATION” field having a plurality of records eachincluding a “BLOOD GLUCOSE LEVEL RANGE” field and a “PRESCRIPTION” fieldis provided, each one record can be configured by a “PATIENT ID” field,a “CLASSIFICATION NUMBER” field, a “DRUG NAME” field and a“CLASSIFICATION INFORMATION” field. By configuring the prescriptioninformation table 1502 by such fields, number of the “PATIENT ID”fields, the “CLASSIFICATION NUMBER” fields and the “DRUG NAME” fieldhaving the same value can be reduced.

Further, by arranging the records in the order of the patient table 1109and referring to the value of the “PRESCRIPTION NUMBER” field, the“PATIENT ID” field can be omitted.

-   (5) The configuration of the fields of the measurement/prescription    table 1602 is not limited to the configuration shown in FIG. 16A.

If the fields of the prescription information table 1502 are configuredin a manner in which the classification number of the patient ID can begrasped by narrowing down with the patient ID as shown in FIG. 16C, the“PRESCRIPTION NUMBER” field of the measurement/prescription table 1602can be omitted.

The information about what concrete operations the user of the bloodglucose meter should perform on the patient is stored in themeasurement/prescription table 1602 and the prescription informationtable 1502, such as whether or not the user should perform blood glucosemeasurement on the patient, whether or not the user should performinsulin administration on the patient, what dosage of insulin should beadministered to the patient when performing insulin administration, andthe like. The configuration of the fields of themeasurement/prescription table 1602 and the prescription informationtable 1502 is not limited to the configuration shown in FIGS. 16A and16C, but can be others as long as “the information about what concreteoperations the user of the blood glucose meter should perform on thepatient” can be correctly expressed.

The blood glucose meter has been disclosed in the present embodiment.

The blood glucose measurement flag is set to “true”, and the bloodglucose level and the patient ID is recorded in themeasurement/prescription results table.

Thereafter, when selecting the “NEXT PATIENT”, in “false” state, therecord of the next patient is recorded in the measurement/prescriptionresults table in the same manner while the insulin administrationconfirmation flag keeps in “false” state.

After the blood glucose measurement performed on the patient has beencompleted, when scanning the patient ID again, a record of the patientID will be found in the measurement/prescription results table, whereinthe record shows that the “BLOOD GLUCOSE MEASUREMENT FLAG” field is“true” and the “INSULIN ADMINISTRATION CONFIRMATION FLAG” field is“false”. Further, after searching the prescription information table1502 with the blood glucose level to obtain the prescription data, thedata is displayed on the display unit.

Owing to this function, “collective measurement and collectiveprescription” can be achieved safely, reliably and rapidly.

Once the insulin dosage display flag is set to “true”, even if the bloodglucose measurement is performed on the patient again by mistake, thescreen page for performing insulin administration will not be displayedagain.

Owing to this function, it is possible to reliably prevent the accidentof duplicated administration of insulin.

Although the present embodiment of the present invention is describedabove, it should be noted that the present invention is not limited tothe above embodiment but includes various other modifications andapplications without departing from the spirit of the claims of thepresent invention.

Explanation of Reference Numerals

101 blood glucose measuring system

102 blood glucose meter (blood glucose measuring device)

103 cradle

104 measurement data management device

105 USB cable

202 optical measuring section

212 measuring tip

204 power switch

205 Cursor keys

206 Enter key

207 Bar-code key

208 bar-code reader

203 LCD

209 power terminal

210 infrared communication window

211 battery lid

302 eject lever

402 charging terminal

403 infrared communication window

619, 719 infrared light-emitting diode

620, 720 phototransistor

602 CPU

603 ROM

605 bus

606 thermistor

607 calendar clock

608 operating section

609 light-emitting diode

610 driver

611 D/A converter

612 phototransistor

613 A/D converter

614 nonvolatile storage

615 display unit

616 buzzer

617 infrared communication section

618 power circuit

702 CPU

703 ROM

704 RAM

717 infrared communication section

706 USB interface

718 charging circuit

705 bus

902 bus

903 CPU

904 ROM

905 RAM

906 nonvolatile storage

907 display unit

908 USB interface

909 operating section

1002 measurement condition check section

1003 blood glucose measuring section

1004 prescription data display section

1007 data communicating section

1103 QC check section

1104 predetermined date interval value

1105 QC check record

1106 judging section

1107 patient ID reading section

1108 patient ID variable

1109 patient table

1110 search section

1111 user ID reading section

1112 user ID variable

1113 user table

1114 search section

1115 tip lot reading section

1116 tip lot variable

1117 tip lot table

1118 judging section

1119 temperature check section

1120 temperature judging section

1122 temperature variable

1123 tip attachment check section

1124 tip attachment detection section

1125 adjustment value

1127 test piece

1128 control section

1202, 1203 comparator

1204 upper limit

1205 lower limit

1206 AND gate

1302, 1303 sample-and-hold circuit

1304 clock

1305 comparator

1306 switch

1307 comparator

1308 threshold

1309 rising edge detection section

1402 adjustment value data

1403 switch

1404 detection section

1405 blood glucose level variable

1406 judging section

1407 recording section

1408 measurement/prescription results table

1502 prescription information table

1503, 1505 search section

1506 blood glucose measurement value

1602 measurement/prescription table

2202 nurse

2203 measuring tip

2204 insulin syringe

2205 patient

2306 patient ID

2307 nurse ID

2308 tip lot

2309 box

2402 fingertip

2403 puncture tool

2710 other patient

1. A blood glucose measuring device comprising: a patient ID readingsection for acquiring a patient ID assigned to a patient; a bloodglucose measuring section for measuring blood glucose level of the blooddrawn from the patient; a nonvolatile storage for storing predetermineddata; a prescription information table stored in the nonvolatilestorage, the prescription information table having prescriptioninformation stored therein in a manner in which the prescriptioninformation can be identified by the patient ID, the prescriptioninformation including kind and dosage of drugs for being administeredcorresponding to the blood glucose level of each of a plurality ofpatients; a search section for searching, with blood glucose level andthe patient ID, the prescription information table to acquire theprescription information of the patient; a display unit for displayingthe prescription information acquired by the search section; anoperating section for allowing an operator to input, in a state wherethe prescription information is displayed on the display unit, whetherthe prescription has been executed or not; and ameasurement/prescription results table stored in the nonvolatilestorage, the measurement/prescription results table having: a patient IDfield having the patient ID acquired by the patient ID reading sectionstored therein, a blood glucose level field for recording the bloodglucose level of the patient measured by the blood glucose measuringsection, a blood glucose measurement flag field for recording whetherthe blood glucose has been measured by the blood glucose measuringsection or not, and an insulin administration confirmation flag fieldfor recording whether the prescription has been executed or not afterthe prescription information has been displayed by the display unit; theblood glucose measuring device further comprising: a recording section;and a control section, wherein, when obtaining the blood glucose levelfrom the blood glucose measuring section, the recording section recordsthe blood glucose level in the blood glucose level field and records alogical true in the blood glucose measurement flag field of a record ofthe measurement/prescription results table, the record being identifiedby the patient ID, while when obtaining operation information from theoperating section, the recording section records a logical true in theinsulin administration confirmation flag field of the record, wherein,after obtaining the patient ID by the patient ID reading section, thecontrol section confirms the blood glucose measurement flag field andthe insulin administration confirmation flag field of the record, and ifthe blood glucose measurement flag field of the record is “true” and theinsulin administration confirmation flag field of the record is “false”,the control section will control the search section to obtain theprescription information, while if the blood glucose measurement flagfield of the record is “true” and the insulin administrationconfirmation flag field of the record is “true”, the control sectionwill not control the search section to obtain the prescriptioninformation; and wherein, upon receipt of an indication to perform bloodglucose measurement, the control section is configured to set the bloodglucose measurement flag field to a logical false and the insulinadministration confirmation flag field to a logical false.
 2. The bloodglucose measuring device according to claim 1, wherein the prescriptioninformation table outputs a plurality of pieces of prescriptioninformation with respect to one blood glucose level obtained by theblood glucose measuring section; wherein the measurement/prescriptionresults table has a plurality of the insulin administration confirmationflag fields, the number of the insulin administration confirmation flagfields being equal to the number of the pieces of prescriptioninformation outputted by the prescription information table; andwherein, in the case where there are a plurality of insulinadministration confirmation flag fields in one record of themeasurement/prescription results table, the control section does notcontrol the search section to acquire the prescription information onlywhen all of the insulin administration confirmation flag fields are“true”.
 3. The blood glucose measuring device according to claim 2,further comprising: a communication section for performing datacommunication with a computer system storing the prescriptioninformation table therein in an editable manner; and ameasurement/prescription table transmitted from the computer system andstored in the nonvolatile storage through the communication section, themeasurement/prescription table including a patient ID field having thepatient ID stored therein, a blood glucose measurement flag field forproviding the indication to perform blood glucose measurement, and aprescription number field having the number of the kind of the drugs forbeing administered to the patient stored therein, wherein, whenreceiving the measurement/prescription table from the computer system,the control section creates the measurement/prescription results tablein the nonvolatile storage according to the content of themeasurement/prescription table.
 4. A blood glucose measuring devicecomprising: a patient ID reading section for acquiring a patient IDassigned to a patient; a blood glucose measuring section for measuringthe blood glucose level of the blood drawn from the patient; anonvolatile storage for storing predetermined data; a prescriptioninformation table stored in the nonvolatile storage, the prescriptioninformation table having prescription information stored therein in amanner in which the prescription information can be identified by thepatient ID, the prescription information including kind and dosage ofdrugs for being administered corresponding to the blood glucose level ofeach of a plurality of patients; a search section for searching, withblood glucose level and the patient ID, the prescription informationtable to acquire the prescription information of the patient; a displayunit for displaying the prescription information acquired by the searchsection; an operating section for allowing an operator to input, in astate where the prescription information is displayed on the displayunit, whether the prescription has been executed or not; ameasurement/prescription results table stored in the nonvolatilestorage, the measurement/prescription results table having: a patient IDfield having the patient ID stored therein, a blood glucose level fieldfor recording the blood glucose level of the patient measured by theblood glucose measuring section, a blood glucose measurement flag fieldfor recording whether the blood glucose has been measured by the bloodglucose measuring section or not, and an insulin administrationconfirmation flag field for recording whether the prescription has beenexecuted or not after the prescription information has been displayed bythe display unit; a recording section; and a control section, wherein,when obtaining the blood glucose level from the blood glucose measuringsection, the recording section records the blood glucose level in theblood glucose level field and records a logical true in the bloodglucose measurement flag field of a record of themeasurement/prescription results table, the record being identified bythe patient ID, while when obtaining operation information from theoperating section, the recording section records a logical true in theinsulin administration confirmation flag field of the record, wherein,after reading the patient ID by the patient ID reading section, if theblood glucose measurement flag field of the record is “true” and theinsulin administration confirmation flag field of the record is “false”,the control section will cause the search section to search theprescription information table with the blood glucose level recorded inthe blood glucose level field of the record and the patient ID toacquire the prescription information and cause the display unit todisplay the prescription information; and wherein, upon receipt of anindication to perform blood glucose measurement, the control section isconfigured to set the blood glucose measurement flag field to a logicalfalse and the insulin administration confirmation flag field to alogical false.
 5. The blood glucose measuring device according to claim4, wherein the prescription information table outputs a plurality ofpieces of prescription information with respect to one blood glucoselevel obtained by the blood glucose measuring section for each differentdrug; wherein the measurement/prescription results table has a pluralityof the insulin administration confirmation flag fields, the number ofthe insulin administration confirmation flag fields being equal to thenumber of the pieces of prescription information outputted by theprescription information table; and wherein, in the case where there area plurality of insulin administration confirmation flag fields in onerecord of the measurement/prescription results table, the controlsection will cause the search section to acquire the prescriptioninformation and cause the display unit to display the prescriptioninformation if either one of the insulin administration confirmationflag fields is “false”.
 6. The blood glucose measuring device accordingto claim 5, further comprising: a communication section for performingdata communication with a computer system storing the prescriptioninformation table therein in an editable manner; and ameasurement/prescription table transmitted from the computer system andstored in the nonvolatile storage through the communication section, themeasurement/prescription table including a patient ID field having thepatient ID stored therein, a blood glucose measurement flag field forproviding the indication to perform blood glucose measurement, and aprescription number field having the number of the kind of the drugs forbeing administered to the patient stored therein, wherein, whenreceiving the measurement/prescription table from the computer system,the control section creates the measurement/prescription results tablein the nonvolatile storage according to the content of themeasurement/prescription table.
 7. A blood glucose measuring methodcomprising: a first step of acquiring a patient ID assigned to apatient; a second step of receiving an indication to perform bloodglucose measurement and measuring the blood glucose level of the blooddrawn from the patient whose patient ID has been acquired in the firststep; and a third step of recording the blood glucose level measured inthe second step in a blood glucose level field of a record of ameasurement/prescription results table stored in a nonvolatile storage,the record being identified by the patient ID, and recording a logicaltrue in a blood glucose measurement flag field of the record, whereinthe measurement/prescription results table includes: a patient ID fieldhaving the patient ID acquired in the first step stored therein, theblood glucose level field for recording the blood glucose level of thepatient measured in the second step, the blood glucose measurement flagfield for recording whether blood glucose has been measured in thesecond step or not, and an insulin administration confirmation flagfield for recording whether the prescription has been executed or not,wherein, upon receipt of the indication to perform blood glucosemeasurement, the blood glucose measurement flag field is set to alogical false and the insulin administration confirmation flag field isset to a logical false.
 8. The blood glucose measuring method accordingto claim 7, further comprising a fourth step which includes: searching aprescription information table stored in the nonvolatile storage withthe patient ID and the blood glucose level to obtain prescriptioninformation of the patient and displaying the obtained prescriptioninformation on a predetermined display unit if a logical value recordedin the blood glucose measurement flag field of the record is “true” anda logical value recorded in the insulin administration confirmation flagfield of the record is “false”, and not obtaining the prescriptioninformation from the prescription information table if the logical valuerecorded in the blood glucose measurement flag field of the record is“true” and the logical value recorded in the insulin administrationconfirmation flag field of the record is “true”, thereby preventing anaccidental duplicate administration of insulin, wherein the prescriptioninformation table has the prescription information stored therein in amanner in which the prescription information can be identified by thepatient ID, and the prescription information includes kind and dosage ofdrugs for being administered corresponding to the blood glucose level ofeach of a plurality of patients.
 9. A blood glucose measuring methodcomprising: a first step of acquiring a patient ID assigned to apatient; a second step of confirming logical values recorded in a bloodglucose measurement flag field and an insulin administrationconfirmation flag field of a record of a measurement/prescriptionresults table stored in a nonvolatile storage, the record beingidentified by the patient ID; and a third step which includes: searchinga prescription information table stored in the nonvolatile storage witha blood glucose level recorded in a blood glucose level field of therecord identified in the second step and the patient ID to obtainprescription information of the patient and displaying the obtainedprescription information on a display unit if it is confirmed in thesecond step that the logical value recorded in the blood glucosemeasurement flag field of the record is “true” and the logical valuerecorded in the insulin administration confirmation flag field of therecord is “false”, wherein the prescription information from theprescription information table of the patient is not displayed on thepanel if the logical value recorded in the blood glucose measurementflag field of the record is “true” and the logical value recorded in theinsulin administration confirmation flag field of the record is “true”,thereby preventing an accidental duplicate administration of insulin,wherein the measurement/prescription results table includes: a patientID field having the patient ID acquired in the second step storedtherein, the blood glucose level field for recording the blood glucoselevel of the patient measured by the blood glucose measuring section,the blood glucose measurement flag field for recording whether the bloodglucose has been measured by the blood glucose measuring section or not,and the insulin administration confirmation flag field for recordingwhether the prescription has been executed or not; wherein theprescription information table has the prescription information storedtherein in a manner in which the prescription information can beidentified by the patient ID; and wherein the prescription informationincludes kind and dosage of drugs for being administered correspondingto the blood glucose level of each of a plurality of patients.